Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_provenance.
- NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_assertion description "[The V198M mutation in the CIAS1 gene was identified in one patient with typical BD but no symptoms of CAPS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_provenance.
- NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_assertion evidence source_evidence_literature NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_provenance.
- NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_assertion SIO_000772 17213252 NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_provenance.
- NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_assertion wasDerivedFrom befree-2016 NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_provenance.
- NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_assertion wasGeneratedBy ECO_0000203 NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_provenance.
- befree-2016 importedOn "2016-02-19" NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_provenance.