Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_provenance.
- NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_assertion description "[We know of no other case of a patient with a disease thought to be unrelated to Duchenne/Becker dystrophy yet demonstrating dystrophin deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_provenance.
- NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_assertion evidence source_evidence_literature NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_provenance.
- NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_assertion SIO_000772 2674948 NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_provenance.
- NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_assertion wasDerivedFrom befree-2016 NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_provenance.
- NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_assertion wasGeneratedBy ECO_0000203 NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295906.RAuFwFhOAemL1QwQjQsvDTjRS__wVGfYbf6My_hptexbo130_provenance.