Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_provenance.
- NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_assertion description "[Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_provenance.
- NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_assertion evidence source_evidence_literature NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_provenance.
- NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_assertion SIO_000772 16648375 NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_provenance.
- NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_assertion wasDerivedFrom befree-20140225 NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_provenance.
- NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_assertion wasGeneratedBy ECO_0000203 NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP441179.RA9ID4gIm8d6NbiBnypwvlTG_2b3jRZ80lduG9xtCVWo0130_provenance.