Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_provenance.
- NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_assertion description "[We aim to identify molecular defects present in the ATP6V1B1, ATP6V0A4 and SLC4A1 genes in a Tunisian cohort, according to the following algorithm: first, ATP6V1B1 gene analysis in dRTA patients with sensorineural hearing loss (SNHL) or unknown hearing status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_provenance.
- NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_assertion evidence source_evidence_literature NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_provenance.
- NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_assertion SIO_000772 24252324 NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_provenance.
- NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_assertion wasDerivedFrom befree-20140225 NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_provenance.
- NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_assertion wasGeneratedBy ECO_0000203 NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP352672.RAdmmXRcjrc4eoUgEicc68OrBqBvmxiXzXebt1xGNsI0Y130_provenance.