Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_provenance.
- NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_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." NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_provenance.
- NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_assertion evidence source_evidence_literature NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_provenance.
- NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_assertion SIO_000772 23335809 NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_provenance.
- NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_assertion wasDerivedFrom befree-20140225 NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_provenance.
- NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_assertion wasGeneratedBy ECO_0000203 NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_provenance.