Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_provenance.
- NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_assertion description "[PTEN hamartoma tumour syndrome (PHTS) encompasses several clinical syndromes with germline mutations in the PTEN tumour suppressor gene, including Cowden syndrome which is characterised by an increased risk of breast and thyroid cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_provenance.
- NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_assertion evidence source_evidence_literature NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_provenance.
- NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_assertion SIO_000772 23335809 NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_provenance.
- NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_assertion wasDerivedFrom befree-2016 NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_provenance.
- NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_assertion wasGeneratedBy ECO_0000203 NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1045499.RAC3o0qtnFoTFNCPDjIwMMO0Ac9goMdupIRduY50J8CZs130_provenance.