Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_provenance.
- NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_assertion wasGeneratedBy ECO_0000203 NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_provenance.
- NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_assertion wasDerivedFrom befree-20150227 NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_provenance.
- NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_assertion SIO_000772 22348646 NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_provenance.
- NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_assertion evidence source_evidence_literature NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_provenance.
- NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_assertion description "[Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865417.RAVLrIpPBkMQQbZu-D_RQV3ULg4iyD5pYJr8_OjIRMVdY130_provenance.