Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_provenance.
- NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_assertion description "[Patients with nemaline myopathy secondary to mutations in the skeletal muscle alpha-actin (ACTA1) gene showed diffuse involvement of thigh and leg muscles with relative sparing of the gastrocnemii.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_provenance.
- NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_assertion evidence source_evidence_literature NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_provenance.
- NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_assertion SIO_000772 15564032 NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_provenance.
- NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_assertion wasDerivedFrom befree-2016 NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_provenance.
- NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_assertion wasGeneratedBy ECO_0000203 NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_provenance.
- befree-2016 importedOn "2016-02-19" NP470182.RABDRK2Lgc9_YS6qRYn8MEOnCyCt0InFgYP5eZvRmWdkw130_provenance.