Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_provenance.
- NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_assertion description "[Limb-girdle muscular dystrophy type 1D (LGMD1D) was linked to chromosome 7q36 over a decade ago, but its genetic cause has remained elusive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_provenance.
- NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_assertion evidence source_evidence_literature NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_provenance.
- NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_assertion SIO_000772 22366786 NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_provenance.
- NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_assertion wasDerivedFrom befree-2016 NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_provenance.
- NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_assertion wasGeneratedBy ECO_0000203 NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_provenance.
- befree-2016 importedOn "2016-02-19" NP963442.RAAEp523sEICTIvh-EcRV0Lu2fC-QmK3d43Rd1Vx4gilc130_provenance.