Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_provenance.
- NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_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." NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_provenance.
- NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_assertion evidence source_evidence_literature NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_provenance.
- NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_assertion SIO_000772 22509993 NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_provenance.
- NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_assertion wasDerivedFrom befree-20150227 NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_provenance.
- NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_assertion wasGeneratedBy ECO_0000203 NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP256862.RA_BzKwbJ0WRS8EsT8AlZRdGPY0bvVWNbmg6q1VvPlNiI130_provenance.