Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_provenance.
- NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_assertion description "[Spectrum of MEK1 and MEK2 gene mutations in cardio-facio-cutaneous syndrome and genotype-phenotype correlations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_provenance.
- NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_assertion evidence source_evidence_literature NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_provenance.
- NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_assertion SIO_000772 19156172 NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_provenance.
- NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_assertion wasDerivedFrom befree-2016 NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_provenance.
- NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_assertion wasGeneratedBy ECO_0000203 NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_provenance.
- befree-2016 importedOn "2016-02-19" NP715604.RAAROOzclHVgTszPf9bXl4XfIMLt8Vde_hOlaeZR0XvBc130_provenance.