Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_provenance.
- NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_assertion description "[Multiple DGC cases in a family, DGC at a young age in an individual or the combination of DGC andlobular breast cancer (LBC) in an individual or a family define the hereditary DGC syndrome (HDGC), and testing for germline CDH1 mutations is warranted in HDGC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_provenance.
- NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_assertion evidence source_evidence_literature NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_provenance.
- NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_assertion SIO_000772 23709761 NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_provenance.
- NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_assertion wasDerivedFrom befree-20140225 NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_provenance.
- NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_assertion wasGeneratedBy ECO_0000203 NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP432263.RAwxoeUBw9nc8ZstCAbEfubeYtqMDn-EOM3ZeIysQxPbk130_provenance.