Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_provenance.
- NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_assertion wasGeneratedBy ECO_0000203 NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_provenance.
- NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_assertion wasDerivedFrom lhgdn-20090331 NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_provenance.
- NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_assertion SIO_000772 18595666 NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_provenance.
- NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_assertion evidence source_evidence_literature NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_provenance.
- NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_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." NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_provenance.