| pubmed-article:21254931 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C2349001 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C1524069 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C0681850 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C1706203 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C2697811 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C0684224 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C0238767 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C1413365 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C1744681 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C0266444 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C1550501 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:21254931 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:21254931 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:21254931 | pubmed:dateCreated | 2011-5-12 | lld:pubmed |
| pubmed-article:21254931 | pubmed:abstractText | Congenital bilateral absence of vas deferens (CBAVD) is a form of male infertility in which mutations occur in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The molecular basis of CBAVD is not completely understood, especially in developing countries. | lld:pubmed |
| pubmed-article:21254931 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21254931 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21254931 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21254931 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21254931 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21254931 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21254931 | pubmed:month | May | lld:pubmed |
| pubmed-article:21254931 | pubmed:issn | 1945-0257 | lld:pubmed |
| pubmed-article:21254931 | pubmed:author | pubmed-author:SaxenaRenuR | lld:pubmed |
| pubmed-article:21254931 | pubmed:author | pubmed-author:VermaIshwar... | lld:pubmed |
| pubmed-article:21254931 | pubmed:author | pubmed-author:MajumdarAbhaA | lld:pubmed |
| pubmed-article:21254931 | pubmed:author | pubmed-author:SachdevaKabir... | lld:pubmed |
| pubmed-article:21254931 | pubmed:author | pubmed-author:ChadhaSudhirS | lld:pubmed |
| pubmed-article:21254931 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21254931 | pubmed:volume | 15 | lld:pubmed |
| pubmed-article:21254931 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21254931 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21254931 | pubmed:pagination | 307-12 | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:meshHeading | pubmed-meshheading:21254931... | lld:pubmed |
| pubmed-article:21254931 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21254931 | pubmed:articleTitle | Mutation studies in the CFTR gene in Asian Indian subjects with congenital bilateral absence of vas deferens: report of two novel mutations and four novel variants. | lld:pubmed |
| pubmed-article:21254931 | pubmed:affiliation | Sir Ganga Ram Hospital, Guru Gobind Singh Indraprastha University, Kashmere Gate, New Delhi, India. kabirtaurus@yahoo.com | lld:pubmed |
| pubmed-article:21254931 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21254931 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:1080 | entrezgene:pubmed | pubmed-article:21254931 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:21254931 | lld:entrezgene |
