Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_provenance.
- NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_assertion description "[identification of three new CNGA3 mutations in patients with achromatopsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_provenance.
- NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_assertion evidence source_evidence_literature NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_provenance.
- NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_assertion SIO_000772 18445228 NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_provenance.
- NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_assertion wasDerivedFrom lhgdn-20090331 NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_provenance.
- NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_assertion wasGeneratedBy ECO_0000203 NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP150915.RADi4FD-1jzRguGQHIwlO6G2rFWCwfWGaBbDk8BELb7T0130_provenance.