Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_provenance.
- NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_assertion description "[Homozygous and compound heterozygous mutations in the ATP6V1B1 gene in patients with renal tubular acidosis and sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_provenance.
- NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_assertion evidence source_evidence_literature NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_provenance.
- NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_assertion SIO_000772 22509993 NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_provenance.
- NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_assertion wasDerivedFrom befree-2016 NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_provenance.
- NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_assertion wasGeneratedBy ECO_0000203 NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_provenance.
- befree-2016 importedOn "2016-02-19" NP975511.RApRbnOVBaHbj8MspxZlMRe6b8CucFFeLzod3KQC9qDuo130_provenance.