Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_provenance.
- NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_assertion description "[Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_provenance.
- NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_assertion evidence source_evidence_literature NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_provenance.
- NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_assertion SIO_000772 23830518 NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_provenance.
- NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_assertion wasDerivedFrom befree-20140225 NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_provenance.
- NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_assertion wasGeneratedBy ECO_0000203 NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP387061.RA7hj1ZK4tfKpEhC0cpDwOV1bWZTk_RoXiebklFoU3YYo130_provenance.