Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_assertion> ?p ?o ?g. }
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- NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_assertion type Assertion NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_head.
- NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_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." NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_provenance.
- NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_assertion evidence source_evidence_literature NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_provenance.
- NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_assertion SIO_000772 23335809 NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_provenance.
- NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_assertion wasDerivedFrom befree-20150227 NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_provenance.
- NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_assertion wasGeneratedBy ECO_0000203 NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_provenance.