Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_provenance.
- NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_assertion description "[resequencing analysis does not support the existence of deleterious, gain-of-function or transcription mutations in HSD17B1, which could explain the clustering of breast cancer cases in non-BRCA1/2 high-risk French Canadian families ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_provenance.
- NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_assertion evidence source_evidence_literature NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_provenance.
- NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_assertion SIO_000772 18083510 NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_provenance.
- NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_assertion wasDerivedFrom lhgdn-20090331 NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_provenance.
- NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_assertion wasGeneratedBy ECO_0000203 NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP232302.RAgexJl2VoucjHMDlQ5ouUuDfrXvrnQG0JoMsRKL1hQ0s130_provenance.