Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_provenance.
- NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_assertion description "[Mutations in GPR54 cause autosomal recessive idiopathic hypogonadotropic hypogonadism in humans and mice, suggesting that this receptor is essential for normal gonadotropin-releasing hormone physiology and for puberty.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_provenance.
- NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_assertion evidence source_evidence_literature NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_provenance.
- NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_assertion SIO_000772 14573733 NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_provenance.
- NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_assertion wasDerivedFrom lhgdn-20090331 NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_provenance.
- NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_assertion wasGeneratedBy ECO_0000203 NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP147018.RA8RlbbXw0QWpqbTktGZXtrbZNm5HgjJi5bWFAreN9ivQ130_provenance.