Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_provenance.
- NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_assertion description "[Furthermore, NR5A1 mutations have now been found in women with familial and sporadic 46,XX primary ovarian insufficiency without adrenal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_provenance.
- NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_assertion evidence source_evidence_literature NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_provenance.
- NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_assertion SIO_000772 20595937 NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_provenance.
- NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_assertion wasDerivedFrom befree-2016 NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_provenance.
- NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_assertion wasGeneratedBy ECO_0000203 NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_provenance.
- befree-2016 importedOn "2016-02-19" NP823081.RATV6vKYMWW7pwN1spUqBB12r7C3vkKBP9TkPt-vu4viw130_provenance.