Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_assertion> ?p ?o ?g. }
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- NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_assertion type Assertion NP587985.RA6IGQWPZJWRdnxdfGIN_M3UdTRBolCJv000_-CKqfg24130_head.
- 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.