Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_provenance.
- NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_assertion description "[Germ line mutations of the BRCA2 tumor suppressor gene with subsequent loss of the remaining wild-type BRCA2 allele have been identified in up to 35% of familial breast cancer cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_provenance.
- NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_assertion evidence source_evidence_literature NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_provenance.
- NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_assertion SIO_000772 18095987 NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_provenance.
- NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_assertion wasDerivedFrom befree-2016 NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_provenance.
- NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_assertion wasGeneratedBy ECO_0000203 NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_provenance.
- befree-2016 importedOn "2016-02-19" NP646492.RA2O7dr5xsPTfw429VQPmqH-o7l-4rX7lgo8ejQXgyH5g130_provenance.