Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1997-9-15
pubmed:databankReference
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AJ001637, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08111, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08112, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08113, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08114, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08115, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08116, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08117, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08118, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08119, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08120, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08121, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08122, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08123, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08124, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08125, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08126, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08127, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08128, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08129, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08130, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08131, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08132, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y10196
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1088-9051
pubmed:author
pubmed:issnType
Print
pubmed:volume
7
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
573-85
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:9199930-Cloning, Molecular, pubmed-meshheading:9199930-Codon, Nonsense, pubmed-meshheading:9199930-Exons, pubmed-meshheading:9199930-Female, pubmed-meshheading:9199930-Frameshift Mutation, pubmed-meshheading:9199930-Genetic Variation, pubmed-meshheading:9199930-Humans, pubmed-meshheading:9199930-Hypophosphatemia, Familial, pubmed-meshheading:9199930-Introns, pubmed-meshheading:9199930-Male, pubmed-meshheading:9199930-Molecular Sequence Data, pubmed-meshheading:9199930-Mutation, pubmed-meshheading:9199930-Neprilysin, pubmed-meshheading:9199930-PHEX Phosphate Regulating Neutral Endopeptidase, pubmed-meshheading:9199930-Pedigree, pubmed-meshheading:9199930-Proteins, pubmed-meshheading:9199930-Sequence Analysis, DNA, pubmed-meshheading:9199930-Sequence Deletion, pubmed-meshheading:9199930-Sequence Homology, Nucleic Acid
pubmed:year
1997
pubmed:articleTitle
Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets.
pubmed:affiliation
Max-Planck Institut für Molekulare Genetik, Berlin, Germany. francis@mpimg-berlin-dahlem.mpg.de
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't