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- source_evidence_literature type ECO_0000212 NP1157831.RA5qskYDy6peqHOJ1A0-NTdZq0BQW5GD3geXr56D-CIGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1157831.RA5qskYDy6peqHOJ1A0-NTdZq0BQW5GD3geXr56D-CIGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1157831.RA5qskYDy6peqHOJ1A0-NTdZq0BQW5GD3geXr56D-CIGA130_provenance.
- NP1157831.RA5qskYDy6peqHOJ1A0-NTdZq0BQW5GD3geXr56D-CIGA130_assertion description "[Expanding the clinical phenotype associated with ELOVL4 mutation: study of a large French-Canadian family with autosomal dominant spinocerebellar ataxia and erythrokeratodermia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1157831.RA5qskYDy6peqHOJ1A0-NTdZq0BQW5GD3geXr56D-CIGA130_provenance.
- NP1157831.RA5qskYDy6peqHOJ1A0-NTdZq0BQW5GD3geXr56D-CIGA130_assertion evidence source_evidence_literature NP1157831.RA5qskYDy6peqHOJ1A0-NTdZq0BQW5GD3geXr56D-CIGA130_provenance.
- NP1157831.RA5qskYDy6peqHOJ1A0-NTdZq0BQW5GD3geXr56D-CIGA130_assertion SIO_000772 24566826 NP1157831.RA5qskYDy6peqHOJ1A0-NTdZq0BQW5GD3geXr56D-CIGA130_provenance.
- NP1157831.RA5qskYDy6peqHOJ1A0-NTdZq0BQW5GD3geXr56D-CIGA130_assertion wasDerivedFrom befree-2016 NP1157831.RA5qskYDy6peqHOJ1A0-NTdZq0BQW5GD3geXr56D-CIGA130_provenance.
- NP1157831.RA5qskYDy6peqHOJ1A0-NTdZq0BQW5GD3geXr56D-CIGA130_assertion wasGeneratedBy ECO_0000203 NP1157831.RA5qskYDy6peqHOJ1A0-NTdZq0BQW5GD3geXr56D-CIGA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1157831.RA5qskYDy6peqHOJ1A0-NTdZq0BQW5GD3geXr56D-CIGA130_provenance.