Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_provenance.
- NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_assertion description "[Mutant POU4F3 loses most of its transcriptional activity and most of its ability to bind to DNA/mutation causes autosomal-dominant nonsyndromic hearing loss and eventually leads to hair cell morbidity in affected family H members.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_provenance.
- NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_assertion evidence source_evidence_literature NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_provenance.
- NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_assertion SIO_000772 14585957 NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_provenance.
- NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_assertion wasDerivedFrom lhgdn-20090331 NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_provenance.
- NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_assertion wasGeneratedBy ECO_0000203 NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP120727.RAPQDhwdcIcXxH7zHIxqbvBZ25gAowxw4wVdMPJaXKKy0130_provenance.