Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_provenance.
- NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_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." NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_provenance.
- NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_assertion evidence source_evidence_literature NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_provenance.
- NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_assertion SIO_000772 16648378 NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_provenance.
- NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_assertion wasDerivedFrom befree-20140225 NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_provenance.
- NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_assertion wasGeneratedBy ECO_0000203 NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_provenance.