| pubmed-article:6274023 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:6274023 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
| pubmed-article:6274023 | lifeskim:mentions | umls-concept:C0684249 | lld:lifeskim |
| pubmed-article:6274023 | lifeskim:mentions | umls-concept:C0008633 | lld:lifeskim |
| pubmed-article:6274023 | lifeskim:mentions | umls-concept:C0795806 | lld:lifeskim |
| pubmed-article:6274023 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:6274023 | lifeskim:mentions | umls-concept:C1457869 | lld:lifeskim |
| pubmed-article:6274023 | lifeskim:mentions | umls-concept:C0205369 | lld:lifeskim |
| pubmed-article:6274023 | pubmed:issue | 4529 | lld:pubmed |
| pubmed-article:6274023 | pubmed:dateCreated | 1982-2-25 | lld:pubmed |
| pubmed-article:6274023 | pubmed:abstractText | A specific, acquired chromosomal abnormality (deletion 3p) has been found in at least one chromosome 3 in 100 percent of the metaphases in 12 of 12 cell lines cultured from human small-cell lung cancer tissue and in 2-day tumor culture specimens from three patients. Analysis of the shortest region of overlap shows the deletion to be 3p(14-23). This specific change was not seen in five of five lung cancer cell lines other than small-cell lung cancer or in two lymphoblastoid lines cultured from cells of small-cell lung cancer patients whose tumors had the 3p deletion. | lld:pubmed |
| pubmed-article:6274023 | pubmed:language | eng | lld:pubmed |
| pubmed-article:6274023 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:6274023 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:6274023 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:6274023 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:6274023 | pubmed:issn | 0036-8075 | lld:pubmed |
| pubmed-article:6274023 | pubmed:author | pubmed-author:Whang-PengJJ | lld:pubmed |
| pubmed-article:6274023 | pubmed:author | pubmed-author:GazdarA FAF | lld:pubmed |
| pubmed-article:6274023 | pubmed:author | pubmed-author:BunnP APA | lld:pubmed |
| pubmed-article:6274023 | pubmed:author | pubmed-author:MinnaJ DJD | lld:pubmed |
| pubmed-article:6274023 | pubmed:author | pubmed-author:LeeE CEC | lld:pubmed |
| pubmed-article:6274023 | pubmed:author | pubmed-author:CarneyD NDN | lld:pubmed |
| pubmed-article:6274023 | pubmed:author | pubmed-author:Kao-ShanC SCS | lld:pubmed |
| pubmed-article:6274023 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:6274023 | pubmed:day | 8 | lld:pubmed |
| pubmed-article:6274023 | pubmed:volume | 215 | lld:pubmed |
| pubmed-article:6274023 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:6274023 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:6274023 | pubmed:pagination | 181-2 | lld:pubmed |
| pubmed-article:6274023 | pubmed:dateRevised | 2007-3-19 | lld:pubmed |
| pubmed-article:6274023 | pubmed:meshHeading | pubmed-meshheading:6274023-... | lld:pubmed |
| pubmed-article:6274023 | pubmed:meshHeading | pubmed-meshheading:6274023-... | lld:pubmed |
| pubmed-article:6274023 | pubmed:meshHeading | pubmed-meshheading:6274023-... | lld:pubmed |
| pubmed-article:6274023 | pubmed:meshHeading | pubmed-meshheading:6274023-... | lld:pubmed |
| pubmed-article:6274023 | pubmed:meshHeading | pubmed-meshheading:6274023-... | lld:pubmed |
| pubmed-article:6274023 | pubmed:meshHeading | pubmed-meshheading:6274023-... | lld:pubmed |
| pubmed-article:6274023 | pubmed:meshHeading | pubmed-meshheading:6274023-... | lld:pubmed |
| pubmed-article:6274023 | pubmed:year | 1982 | lld:pubmed |
| pubmed-article:6274023 | pubmed:articleTitle | Specific chromosome defect associated with human small-cell lung cancer; deletion 3p(14-23). | lld:pubmed |
| pubmed-article:6274023 | pubmed:publicationType | Journal Article | lld:pubmed |
| entrez-gene:7864 | entrezgene:pubmed | pubmed-article:6274023 | lld:entrezgene |
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