Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_provenance.
- NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_assertion description "[Patients with mutations in the ATP6V1B1 proton pump subunit develop dRTA and in most of the cases sensorineural hearing loss early in childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_provenance.
- NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_assertion evidence source_evidence_literature NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_provenance.
- NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_assertion SIO_000772 22509993 NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_provenance.
- NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_assertion wasDerivedFrom befree-20140225 NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_provenance.
- NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_assertion wasGeneratedBy ECO_0000203 NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP832707.RAsEjT3tsLPqtFFAD2FPSPf2ViM5nLt_vwZ0djJZ8W8RU130_provenance.