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- source_evidence_literature type ECO_0000212 NP1005858.RAIAwQxsEyxyAtwZ2TPQy-Z29BVn_53iW97swh0oN2L_4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1005858.RAIAwQxsEyxyAtwZ2TPQy-Z29BVn_53iW97swh0oN2L_4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1005858.RAIAwQxsEyxyAtwZ2TPQy-Z29BVn_53iW97swh0oN2L_4130_provenance.
- NP1005858.RAIAwQxsEyxyAtwZ2TPQy-Z29BVn_53iW97swh0oN2L_4130_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." NP1005858.RAIAwQxsEyxyAtwZ2TPQy-Z29BVn_53iW97swh0oN2L_4130_provenance.
- NP1005858.RAIAwQxsEyxyAtwZ2TPQy-Z29BVn_53iW97swh0oN2L_4130_assertion evidence source_evidence_literature NP1005858.RAIAwQxsEyxyAtwZ2TPQy-Z29BVn_53iW97swh0oN2L_4130_provenance.
- NP1005858.RAIAwQxsEyxyAtwZ2TPQy-Z29BVn_53iW97swh0oN2L_4130_assertion SIO_000772 16648378 NP1005858.RAIAwQxsEyxyAtwZ2TPQy-Z29BVn_53iW97swh0oN2L_4130_provenance.
- NP1005858.RAIAwQxsEyxyAtwZ2TPQy-Z29BVn_53iW97swh0oN2L_4130_assertion wasDerivedFrom befree-20150227 NP1005858.RAIAwQxsEyxyAtwZ2TPQy-Z29BVn_53iW97swh0oN2L_4130_provenance.
- NP1005858.RAIAwQxsEyxyAtwZ2TPQy-Z29BVn_53iW97swh0oN2L_4130_assertion wasGeneratedBy ECO_0000203 NP1005858.RAIAwQxsEyxyAtwZ2TPQy-Z29BVn_53iW97swh0oN2L_4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1005858.RAIAwQxsEyxyAtwZ2TPQy-Z29BVn_53iW97swh0oN2L_4130_provenance.