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- source_evidence_literature type ECO_0000212 NP547528.RA38QEodSWE9_v28OHvuyBkQ4frcyd_2TnoBYlusTOLZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547528.RA38QEodSWE9_v28OHvuyBkQ4frcyd_2TnoBYlusTOLZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547528.RA38QEodSWE9_v28OHvuyBkQ4frcyd_2TnoBYlusTOLZM130_provenance.
- NP547528.RA38QEodSWE9_v28OHvuyBkQ4frcyd_2TnoBYlusTOLZM130_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." NP547528.RA38QEodSWE9_v28OHvuyBkQ4frcyd_2TnoBYlusTOLZM130_provenance.
- NP547528.RA38QEodSWE9_v28OHvuyBkQ4frcyd_2TnoBYlusTOLZM130_assertion evidence source_evidence_literature NP547528.RA38QEodSWE9_v28OHvuyBkQ4frcyd_2TnoBYlusTOLZM130_provenance.
- NP547528.RA38QEodSWE9_v28OHvuyBkQ4frcyd_2TnoBYlusTOLZM130_assertion SIO_000772 16648378 NP547528.RA38QEodSWE9_v28OHvuyBkQ4frcyd_2TnoBYlusTOLZM130_provenance.
- NP547528.RA38QEodSWE9_v28OHvuyBkQ4frcyd_2TnoBYlusTOLZM130_assertion wasDerivedFrom befree-2016 NP547528.RA38QEodSWE9_v28OHvuyBkQ4frcyd_2TnoBYlusTOLZM130_provenance.
- NP547528.RA38QEodSWE9_v28OHvuyBkQ4frcyd_2TnoBYlusTOLZM130_assertion wasGeneratedBy ECO_0000203 NP547528.RA38QEodSWE9_v28OHvuyBkQ4frcyd_2TnoBYlusTOLZM130_provenance.
- befree-2016 importedOn "2016-02-19" NP547528.RA38QEodSWE9_v28OHvuyBkQ4frcyd_2TnoBYlusTOLZM130_provenance.