Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_provenance.
- NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_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." NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_provenance.
- NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_assertion evidence source_evidence_literature NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_provenance.
- NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_assertion SIO_000772 10982030 NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_provenance.
- NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_assertion wasDerivedFrom befree-20150227 NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_provenance.
- NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_assertion wasGeneratedBy ECO_0000203 NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP653763.RAHcFgbsW_YylS8R1yFLtDW_3Rp8uYsFZzF9bPnD9Z6bs130_provenance.