Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP552604.RAvwsITS4ThqWKWv6uRWuV4MSfm9ayG3Dm4xP8lpbsmdA130_assertion> ?p ?o ?g. }
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- NP552604.RAvwsITS4ThqWKWv6uRWuV4MSfm9ayG3Dm4xP8lpbsmdA130_assertion type Assertion NP552604.RAvwsITS4ThqWKWv6uRWuV4MSfm9ayG3Dm4xP8lpbsmdA130_head.
- NP552604.RAvwsITS4ThqWKWv6uRWuV4MSfm9ayG3Dm4xP8lpbsmdA130_assertion description "[These new findings include rare germline mutations in other high penetrant genes, the most important of which include TP53 mutations in Li-Fraumeni syndrome, STK11 mutations in Peutz-Jeghers syndrome, and PTEN mutations in Cowden syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552604.RAvwsITS4ThqWKWv6uRWuV4MSfm9ayG3Dm4xP8lpbsmdA130_provenance.
- NP552604.RAvwsITS4ThqWKWv6uRWuV4MSfm9ayG3Dm4xP8lpbsmdA130_assertion evidence source_evidence_literature NP552604.RAvwsITS4ThqWKWv6uRWuV4MSfm9ayG3Dm4xP8lpbsmdA130_provenance.
- NP552604.RAvwsITS4ThqWKWv6uRWuV4MSfm9ayG3Dm4xP8lpbsmdA130_assertion SIO_000772 23586058 NP552604.RAvwsITS4ThqWKWv6uRWuV4MSfm9ayG3Dm4xP8lpbsmdA130_provenance.
- NP552604.RAvwsITS4ThqWKWv6uRWuV4MSfm9ayG3Dm4xP8lpbsmdA130_assertion wasDerivedFrom befree-20140225 NP552604.RAvwsITS4ThqWKWv6uRWuV4MSfm9ayG3Dm4xP8lpbsmdA130_provenance.
- NP552604.RAvwsITS4ThqWKWv6uRWuV4MSfm9ayG3Dm4xP8lpbsmdA130_assertion wasGeneratedBy ECO_0000203 NP552604.RAvwsITS4ThqWKWv6uRWuV4MSfm9ayG3Dm4xP8lpbsmdA130_provenance.