Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_provenance.
- NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_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." NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_provenance.
- NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_assertion evidence source_evidence_literature NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_provenance.
- NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_assertion SIO_000772 10482271 NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_provenance.
- NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_assertion wasDerivedFrom befree-2016 NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_provenance.
- NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_assertion wasGeneratedBy ECO_0000203 NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP262678.RAVmBvQq5HxuMfPZTYnjoTPSHKNGsA3fd4qs6GacVOzFQ130_provenance.