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- source_evidence_literature type ECO_0000212 NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_provenance.
- NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_assertion description "[To investigate whether Leber's hereditary optic neuropathy (LHON) could be caused by mutations in OPA1 we also screened a panel of 28 LHON patients who tested negatively for the three major LHON mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_provenance.
- NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_assertion evidence source_evidence_literature NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_provenance.
- NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_assertion SIO_000772 11440989 NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_provenance.
- NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_assertion wasDerivedFrom befree-20140225 NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_provenance.
- NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_assertion wasGeneratedBy ECO_0000203 NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_provenance.
- befree-20140225 importedOn "2014-02-25" NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_provenance.