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- source_evidence_literature type ECO_0000212 NP356975.RACVaji1QdJizUqPZGPPxBwGSrOEB7pAtEqpcJizmf0y0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP356975.RACVaji1QdJizUqPZGPPxBwGSrOEB7pAtEqpcJizmf0y0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP356975.RACVaji1QdJizUqPZGPPxBwGSrOEB7pAtEqpcJizmf0y0130_provenance.
- NP356975.RACVaji1QdJizUqPZGPPxBwGSrOEB7pAtEqpcJizmf0y0130_assertion description "[We found a frequent recurrence of mutations in DYNC1H1, implying that this gene is a major locus for unexplained MCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP356975.RACVaji1QdJizUqPZGPPxBwGSrOEB7pAtEqpcJizmf0y0130_provenance.
- NP356975.RACVaji1QdJizUqPZGPPxBwGSrOEB7pAtEqpcJizmf0y0130_assertion evidence source_evidence_literature NP356975.RACVaji1QdJizUqPZGPPxBwGSrOEB7pAtEqpcJizmf0y0130_provenance.
- NP356975.RACVaji1QdJizUqPZGPPxBwGSrOEB7pAtEqpcJizmf0y0130_assertion SIO_000772 23603762 NP356975.RACVaji1QdJizUqPZGPPxBwGSrOEB7pAtEqpcJizmf0y0130_provenance.
- NP356975.RACVaji1QdJizUqPZGPPxBwGSrOEB7pAtEqpcJizmf0y0130_assertion wasDerivedFrom befree-20150227 NP356975.RACVaji1QdJizUqPZGPPxBwGSrOEB7pAtEqpcJizmf0y0130_provenance.
- NP356975.RACVaji1QdJizUqPZGPPxBwGSrOEB7pAtEqpcJizmf0y0130_assertion wasGeneratedBy ECO_0000203 NP356975.RACVaji1QdJizUqPZGPPxBwGSrOEB7pAtEqpcJizmf0y0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP356975.RACVaji1QdJizUqPZGPPxBwGSrOEB7pAtEqpcJizmf0y0130_provenance.