Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_provenance.
- NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_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." NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_provenance.
- NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_assertion evidence source_evidence_literature NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_provenance.
- NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_assertion SIO_000772 19156172 NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_provenance.
- NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_assertion wasDerivedFrom befree-20150227 NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_provenance.
- NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_assertion wasGeneratedBy ECO_0000203 NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP646038.RA8Uc6aifeA9xmfk4Ue8HGHWXVVyyu0NUhvqUNHsD4Riw130_provenance.