Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_provenance.
- NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_assertion wasGeneratedBy ECO_0000203 NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_provenance.
- NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_assertion wasDerivedFrom lhgdn-20090331 NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_provenance.
- NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_assertion SIO_000772 18429043 NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_provenance.
- NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_assertion evidence source_evidence_literature NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_provenance.
- NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_assertion description "[Based on our results it is estimated that about 20% of patients with Usher syndrome type I have CDH23 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210491.RAvGK54UTOVx2h2aktOLA9xv8c7jfKFErWnI3rr3PPk3M130_provenance.