Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_provenance.
- NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_assertion description "[Welander distal myopathy (WDM) is an autosomal dominant myopathy with late-adult onset characterized by slow progression of distal muscle weakness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_provenance.
- NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_assertion evidence source_evidence_literature NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_provenance.
- NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_assertion SIO_000772 10482271 NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_provenance.
- NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_assertion wasDerivedFrom befree-20150227 NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_provenance.
- NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_assertion wasGeneratedBy ECO_0000203 NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP900186.RAAScX9Rw5teaBpjFjijl_j0HfDtarlMXePsENhVbBewM130_provenance.