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- source_evidence_literature type ECO_0000212 NP853322.RA94mmqEn15fct4pNGEU-mw8iN06ELckKh0JgvzX7ON0s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP853322.RA94mmqEn15fct4pNGEU-mw8iN06ELckKh0JgvzX7ON0s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP853322.RA94mmqEn15fct4pNGEU-mw8iN06ELckKh0JgvzX7ON0s130_provenance.
- NP853322.RA94mmqEn15fct4pNGEU-mw8iN06ELckKh0JgvzX7ON0s130_assertion description "[Linkage and sequence mutation analyses of the ADOA candidate genes OPA1, OPA3, OPA4, and OPA5, including the genes WFS1, GJB2, and GJB6 associated with recessive inherited OA or dominant LFSNHL, were performed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853322.RA94mmqEn15fct4pNGEU-mw8iN06ELckKh0JgvzX7ON0s130_provenance.
- NP853322.RA94mmqEn15fct4pNGEU-mw8iN06ELckKh0JgvzX7ON0s130_assertion evidence source_evidence_literature NP853322.RA94mmqEn15fct4pNGEU-mw8iN06ELckKh0JgvzX7ON0s130_provenance.
- NP853322.RA94mmqEn15fct4pNGEU-mw8iN06ELckKh0JgvzX7ON0s130_assertion SIO_000772 16648378 NP853322.RA94mmqEn15fct4pNGEU-mw8iN06ELckKh0JgvzX7ON0s130_provenance.
- NP853322.RA94mmqEn15fct4pNGEU-mw8iN06ELckKh0JgvzX7ON0s130_assertion wasDerivedFrom befree-20150227 NP853322.RA94mmqEn15fct4pNGEU-mw8iN06ELckKh0JgvzX7ON0s130_provenance.
- NP853322.RA94mmqEn15fct4pNGEU-mw8iN06ELckKh0JgvzX7ON0s130_assertion wasGeneratedBy ECO_0000203 NP853322.RA94mmqEn15fct4pNGEU-mw8iN06ELckKh0JgvzX7ON0s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP853322.RA94mmqEn15fct4pNGEU-mw8iN06ELckKh0JgvzX7ON0s130_provenance.