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- source_evidence_literature type ECO_0000212 NP297109.RATr_1rV1JRoptrFkxLdg-ywErnQorwVlbg690i5bu160130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP297109.RATr_1rV1JRoptrFkxLdg-ywErnQorwVlbg690i5bu160130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP297109.RATr_1rV1JRoptrFkxLdg-ywErnQorwVlbg690i5bu160130_provenance.
- NP297109.RATr_1rV1JRoptrFkxLdg-ywErnQorwVlbg690i5bu160130_assertion description "[Among the 60 patients with sporadic ataxias in the present series, 3 (5.0%) were found to harbor SCA3 mutations, whereas none were found to harbor SCA6 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297109.RATr_1rV1JRoptrFkxLdg-ywErnQorwVlbg690i5bu160130_provenance.
- NP297109.RATr_1rV1JRoptrFkxLdg-ywErnQorwVlbg690i5bu160130_assertion evidence source_evidence_literature NP297109.RATr_1rV1JRoptrFkxLdg-ywErnQorwVlbg690i5bu160130_provenance.
- NP297109.RATr_1rV1JRoptrFkxLdg-ywErnQorwVlbg690i5bu160130_assertion SIO_000772 15979648 NP297109.RATr_1rV1JRoptrFkxLdg-ywErnQorwVlbg690i5bu160130_provenance.
- NP297109.RATr_1rV1JRoptrFkxLdg-ywErnQorwVlbg690i5bu160130_assertion wasDerivedFrom befree-20140225 NP297109.RATr_1rV1JRoptrFkxLdg-ywErnQorwVlbg690i5bu160130_provenance.
- NP297109.RATr_1rV1JRoptrFkxLdg-ywErnQorwVlbg690i5bu160130_assertion wasGeneratedBy ECO_0000203 NP297109.RATr_1rV1JRoptrFkxLdg-ywErnQorwVlbg690i5bu160130_provenance.
- befree-20140225 importedOn "2014-02-25" NP297109.RATr_1rV1JRoptrFkxLdg-ywErnQorwVlbg690i5bu160130_provenance.