Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_provenance.
- NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_assertion wasGeneratedBy ECO_0000203 NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_provenance.
- NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_assertion wasDerivedFrom lhgdn-20090331 NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_provenance.
- NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_assertion SIO_000772 16550584 NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_provenance.
- NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_assertion evidence source_evidence_literature NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_provenance.
- NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_assertion description "[Missense mutations within a defined region are associated with dominant low-frequency hearing loss (DFNA6/14/38), while more severe mutations spanning WFS1 are found in Wolfram syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_provenance.