Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_provenance.
- NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_assertion description "[Lack of evidence for frequent MED12 p.L1224F mutation in prostate tumours from Caucasian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_provenance.
- NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_assertion evidence source_evidence_literature NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_provenance.
- NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_assertion SIO_000772 23661306 NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_provenance.
- NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_assertion wasDerivedFrom befree-2016 NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_provenance.
- NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_assertion wasGeneratedBy ECO_0000203 NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1076591.RAHHr6AHD4iPOIdTa0hrQusv3xXn6jdHC8XmfuOV3AdS4130_provenance.