Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_provenance.
- NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_assertion description "[Mutation analysis for autosomal dominant hereditary breast/ovarian cancer genes (BRCA1/BRCA2) became an important technique for women at risk of carrying these mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_provenance.
- NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_assertion evidence source_evidence_literature NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_provenance.
- NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_assertion SIO_000772 11426450 NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_provenance.
- NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_assertion wasDerivedFrom befree-2016 NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_provenance.
- NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_assertion wasGeneratedBy ECO_0000203 NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_provenance.
- befree-2016 importedOn "2016-02-19" NP322066.RAsm502Aq1f7xR3MQrAKXL7MGavlcIE9FNys7DOTzxbPg130_provenance.