Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_provenance.
- NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_assertion description "[A new polymorphism in the coding region of exon four in HSD17B2 in relation to risk of sporadic and hereditary breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_provenance.
- NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_assertion evidence source_evidence_literature NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_provenance.
- NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_assertion SIO_000772 17260097 NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_provenance.
- NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_assertion wasDerivedFrom befree-2016 NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_provenance.
- NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_assertion wasGeneratedBy ECO_0000203 NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_provenance.
- befree-2016 importedOn "2016-02-19" NP591222.RAxTRlHpPmqPBg1SwoLw2Z-VKWuPshGjChydOE65YnI5s130_provenance.