Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_provenance.
- NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_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." NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_provenance.
- NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_assertion evidence source_evidence_literature NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_provenance.
- NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_assertion SIO_000772 19156172 NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_provenance.
- NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_assertion wasDerivedFrom befree-20140225 NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_provenance.
- NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_assertion wasGeneratedBy ECO_0000203 NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP891331.RAlEq3QV0RChIr0iMDdB-gbED9RzmTKZMq0V03i5zswqk130_provenance.