Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_provenance.
- NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_assertion description "[Cowden disease is an autosomal dominant disorder associated with an elevated risk of breast, thyroid and skin cancers, in which germline mutations of a tumour suppressor gene (PTEN) have been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_provenance.
- NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_assertion evidence source_evidence_literature NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_provenance.
- NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_assertion SIO_000772 10982030 NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_provenance.
- NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_assertion wasDerivedFrom befree-20140225 NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_provenance.
- NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_assertion wasGeneratedBy ECO_0000203 NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP916676.RAgXo2jzSIzbaQ1JhCxZRH4R0pC1bNdQ6zR1ksCTEc-vU130_provenance.