Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_provenance.
- NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_assertion wasGeneratedBy ECO_0000203 NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_provenance.
- NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_assertion wasDerivedFrom lhgdn-20090331 NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_provenance.
- NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_assertion SIO_000772 15563506 NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_provenance.
- NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_assertion evidence source_evidence_literature NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_provenance.
- NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_assertion description "[dominant mutations are common in Ullrich congenital muscular dystrophy (UCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208223.RASavEzrvF3jlJp9RJrYU2MfkTFXICFxQp0TUJc0Udc8U130_provenance.