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- source_evidence_literature type ECO_0000212 NP898112.RAvn0i6FBVmSW7UxjlBPYej8eXqnBlm7--bFNhz8GhLR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP898112.RAvn0i6FBVmSW7UxjlBPYej8eXqnBlm7--bFNhz8GhLR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP898112.RAvn0i6FBVmSW7UxjlBPYej8eXqnBlm7--bFNhz8GhLR0130_provenance.
- NP898112.RAvn0i6FBVmSW7UxjlBPYej8eXqnBlm7--bFNhz8GhLR0130_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." NP898112.RAvn0i6FBVmSW7UxjlBPYej8eXqnBlm7--bFNhz8GhLR0130_provenance.
- NP898112.RAvn0i6FBVmSW7UxjlBPYej8eXqnBlm7--bFNhz8GhLR0130_assertion evidence source_evidence_literature NP898112.RAvn0i6FBVmSW7UxjlBPYej8eXqnBlm7--bFNhz8GhLR0130_provenance.
- NP898112.RAvn0i6FBVmSW7UxjlBPYej8eXqnBlm7--bFNhz8GhLR0130_assertion SIO_000772 24252324 NP898112.RAvn0i6FBVmSW7UxjlBPYej8eXqnBlm7--bFNhz8GhLR0130_provenance.
- NP898112.RAvn0i6FBVmSW7UxjlBPYej8eXqnBlm7--bFNhz8GhLR0130_assertion wasDerivedFrom befree-20150227 NP898112.RAvn0i6FBVmSW7UxjlBPYej8eXqnBlm7--bFNhz8GhLR0130_provenance.
- NP898112.RAvn0i6FBVmSW7UxjlBPYej8eXqnBlm7--bFNhz8GhLR0130_assertion wasGeneratedBy ECO_0000203 NP898112.RAvn0i6FBVmSW7UxjlBPYej8eXqnBlm7--bFNhz8GhLR0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP898112.RAvn0i6FBVmSW7UxjlBPYej8eXqnBlm7--bFNhz8GhLR0130_provenance.