Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_provenance.
- NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_assertion description "[Clinical review of known individuals with MEK1/MEK2 mutations suggests that these patients show dysmorphic features, ectodermal abnormalities and cognitive deficit similar to what was observed in BRAF-mutated patients and in the general CFCS population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_provenance.
- NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_assertion evidence source_evidence_literature NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_provenance.
- NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_assertion SIO_000772 19156172 NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_provenance.
- NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_assertion wasDerivedFrom befree-20140225 NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_provenance.
- NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_assertion wasGeneratedBy ECO_0000203 NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP592580.RAeZnO__BCD3QcbDFXvfike-rtg2dBd22nIntdMtuMWKk130_provenance.