Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_provenance.
- NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_assertion description "[Germline CDH1 mutations are not always detectable in patients who meet the HDGC criteria and the aetiological role of this gene is still under investigation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_provenance.
- NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_assertion evidence source_evidence_literature NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_provenance.
- NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_assertion SIO_000772 14630673 NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_provenance.
- NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_assertion wasDerivedFrom befree-20140225 NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_provenance.
- NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_assertion wasGeneratedBy ECO_0000203 NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP288649.RAgdBU6zvJrhL6uGkKaibhcn2C2RMfGL5dFPXwxfCbLgc130_provenance.