Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_provenance.
- NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_assertion description "[Functional analysis of R75Q mutation in the gene coding for Connexin 26 identified in a family with nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_provenance.
- NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_assertion evidence source_evidence_curated NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_provenance.
- NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_assertion SIO_000772 15996214 NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_provenance.
- NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_assertion wasDerivedFrom uniprot-20130724 NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_provenance.
- NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_assertion wasGeneratedBy ECO_0000218 NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP2736.RAaKZhF2uVx4y7nYQSAzJSuqvNiJgBdyPVQPSob58Fxho130_provenance.