Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_provenance.
- NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_assertion wasGeneratedBy ECO_0000203 NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_provenance.
- NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_assertion wasDerivedFrom lhgdn-20090331 NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_provenance.
- NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_assertion SIO_000772 18595666 NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_provenance.
- NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_assertion evidence source_evidence_literature NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_provenance.
- NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_assertion description "[study identified a novel MITF mutation of IVS4 -1G -- > C in a Japanese family with Waardenburg syndrome type II ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP239565.RAUWtK4La_NUpyxsLp0JwvwQIRFnwLhTXR8PwW89-m6R0130_provenance.