Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_provenance.
- NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_assertion description "[Here we screened a cohort of 33 individuals with CFCS for MEK1 and MEK2 gene mutations to further explore their molecular spectrum in this disorder, and to analyze genotype-phenotype correlations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_provenance.
- NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_assertion evidence source_evidence_literature NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_provenance.
- NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_assertion SIO_000772 19156172 NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_provenance.
- NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_assertion wasDerivedFrom befree-20140225 NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_provenance.
- NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_assertion wasGeneratedBy ECO_0000203 NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP805027.RAI1vzoPEc_6wGt2MZMZFe6jqLLXREEnYjG89EqNNMSuQ130_provenance.