Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_provenance.
- NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_provenance.
- NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_assertion evidence source_evidence_literature NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_provenance.
- NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_assertion SIO_000772 18429043 NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_provenance.
- NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_assertion wasDerivedFrom befree-2016 NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_provenance.
- NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_assertion wasGeneratedBy ECO_0000203 NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_provenance.
- befree-2016 importedOn "2016-02-19" NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_provenance.