Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_provenance.
- NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_assertion description "[Lack of functional stereocilin and CATSPER2 (a voltage-gate cation channel expressed specifically in spermatozoa) may explain the observed deafness and male infertility phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_provenance.
- NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_assertion evidence source_evidence_literature NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_provenance.
- NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_assertion SIO_000772 12825070 NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_provenance.
- NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_assertion wasDerivedFrom befree-20140225 NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_provenance.
- NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_assertion wasGeneratedBy ECO_0000203 NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP887610.RA20iI8p2nb3RitsCBfNSX7Z8w6AUglyFZlM08ilHRAMU130_provenance.