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- source_evidence_literature type ECO_0000212 NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_provenance.
- NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_assertion description "[Calpain 3 is the muscle-specific member of the calcium activated neutral protease family and primary mutations in the CAPN3 gene cause limb girdle muscular dystrophy type 2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_provenance.
- NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_assertion evidence source_evidence_literature NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_provenance.
- NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_assertion SIO_000772 11053681 NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_provenance.
- NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_assertion wasDerivedFrom befree-20140225 NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_provenance.
- NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_assertion wasGeneratedBy ECO_0000203 NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP745514.RABV77JwJY17ObnqNwltVhA5mcHVxfhIVpU-cDOYrizsk130_provenance.