Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_assertion> ?p ?o ?g. }
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- NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_assertion type Assertion NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_head.
- NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_assertion wasGeneratedBy ECO_0000218 NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_provenance.
- NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_assertion wasDerivedFrom uniprot-20150221 NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_provenance.
- NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_assertion SIO_000772 10925378 NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_provenance.
- NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_assertion evidence source_evidence_curated NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_provenance.
- NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_assertion description "[Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3021.RAFcxCNpWcfMoqZdAz7_o9-3H1vD3TutOCbicR6sUJ26c130_provenance.