Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_provenance.
- NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_assertion description "[Despite the difference in phenotypes, there remains a possibility that the causative gene for these Japanese SCA is allelic to SCA15.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_provenance.
- NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_assertion evidence source_evidence_literature NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_provenance.
- NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_assertion SIO_000772 14981189 NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_provenance.
- NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_assertion wasDerivedFrom befree-20150227 NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_provenance.
- NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_assertion wasGeneratedBy ECO_0000203 NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP518749.RAbx1LFZEb7jyKsZxJEn91dHi6u8tlOE2knOLxUVRlUmE130_provenance.