Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance.
- NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_assertion description "[Limb-girdle muscular dystrophy 1A (LGMD1A [MIM 159000]) is an autosomal dominant form of muscular dystrophy characterized by adult onset of proximal weakness progressing to distal muscle weakness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance.
- NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_assertion evidence source_evidence_literature NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance.
- NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_assertion SIO_000772 12428213 NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance.
- NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_assertion wasDerivedFrom befree-20150227 NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance.
- NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_assertion wasGeneratedBy ECO_0000203 NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP824731.RATV4FwQev2gl6blliA4Q5kysIX8JIfHtkSC2pcEI0iYo130_provenance.