Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP580319.RA61N1LEnGlGIAH-E6OeIp8yMRJsObt0c_1hXQR6VUnHY130_assertion> ?p ?o ?g. }
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- NP580319.RA61N1LEnGlGIAH-E6OeIp8yMRJsObt0c_1hXQR6VUnHY130_assertion type Assertion NP580319.RA61N1LEnGlGIAH-E6OeIp8yMRJsObt0c_1hXQR6VUnHY130_head.
- NP580319.RA61N1LEnGlGIAH-E6OeIp8yMRJsObt0c_1hXQR6VUnHY130_assertion description "[Two patients had paired mutations in the MVK gene (genotypes V377I/V377I and V377I/S135L) and displayed typical features of BD and MKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580319.RA61N1LEnGlGIAH-E6OeIp8yMRJsObt0c_1hXQR6VUnHY130_provenance.
- NP580319.RA61N1LEnGlGIAH-E6OeIp8yMRJsObt0c_1hXQR6VUnHY130_assertion evidence source_evidence_literature NP580319.RA61N1LEnGlGIAH-E6OeIp8yMRJsObt0c_1hXQR6VUnHY130_provenance.
- NP580319.RA61N1LEnGlGIAH-E6OeIp8yMRJsObt0c_1hXQR6VUnHY130_assertion SIO_000772 17213252 NP580319.RA61N1LEnGlGIAH-E6OeIp8yMRJsObt0c_1hXQR6VUnHY130_provenance.
- NP580319.RA61N1LEnGlGIAH-E6OeIp8yMRJsObt0c_1hXQR6VUnHY130_assertion wasDerivedFrom befree-20150227 NP580319.RA61N1LEnGlGIAH-E6OeIp8yMRJsObt0c_1hXQR6VUnHY130_provenance.
- NP580319.RA61N1LEnGlGIAH-E6OeIp8yMRJsObt0c_1hXQR6VUnHY130_assertion wasGeneratedBy ECO_0000203 NP580319.RA61N1LEnGlGIAH-E6OeIp8yMRJsObt0c_1hXQR6VUnHY130_provenance.