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- source_evidence_literature type ECO_0000212 NP486446.RA5wheiO2Qbgj18pZf-c6chkWsKFid8QJXb8gjMw0WpIE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP486446.RA5wheiO2Qbgj18pZf-c6chkWsKFid8QJXb8gjMw0WpIE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP486446.RA5wheiO2Qbgj18pZf-c6chkWsKFid8QJXb8gjMw0WpIE130_provenance.
- NP486446.RA5wheiO2Qbgj18pZf-c6chkWsKFid8QJXb8gjMw0WpIE130_assertion description "[Accordingly, mutations in these genes are present in a wide variety of spontaneous human cancers and CDKN2A germ line mutations are found in familial melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP486446.RA5wheiO2Qbgj18pZf-c6chkWsKFid8QJXb8gjMw0WpIE130_provenance.
- NP486446.RA5wheiO2Qbgj18pZf-c6chkWsKFid8QJXb8gjMw0WpIE130_assertion evidence source_evidence_literature NP486446.RA5wheiO2Qbgj18pZf-c6chkWsKFid8QJXb8gjMw0WpIE130_provenance.
- NP486446.RA5wheiO2Qbgj18pZf-c6chkWsKFid8QJXb8gjMw0WpIE130_assertion SIO_000772 15781639 NP486446.RA5wheiO2Qbgj18pZf-c6chkWsKFid8QJXb8gjMw0WpIE130_provenance.
- NP486446.RA5wheiO2Qbgj18pZf-c6chkWsKFid8QJXb8gjMw0WpIE130_assertion wasDerivedFrom befree-2016 NP486446.RA5wheiO2Qbgj18pZf-c6chkWsKFid8QJXb8gjMw0WpIE130_provenance.
- NP486446.RA5wheiO2Qbgj18pZf-c6chkWsKFid8QJXb8gjMw0WpIE130_assertion wasGeneratedBy ECO_0000203 NP486446.RA5wheiO2Qbgj18pZf-c6chkWsKFid8QJXb8gjMw0WpIE130_provenance.
- befree-2016 importedOn "2016-02-19" NP486446.RA5wheiO2Qbgj18pZf-c6chkWsKFid8QJXb8gjMw0WpIE130_provenance.