Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP741798.RA7RO3xQlD543-Wi9Guo3wupEUveSQUukrgb0UPC9JsCg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP741798.RA7RO3xQlD543-Wi9Guo3wupEUveSQUukrgb0UPC9JsCg130_assertion type Assertion NP741798.RA7RO3xQlD543-Wi9Guo3wupEUveSQUukrgb0UPC9JsCg130_head.
- NP741798.RA7RO3xQlD543-Wi9Guo3wupEUveSQUukrgb0UPC9JsCg130_assertion description "[Cowden disease (CD) is a genetically heterogeneous inherited cancer syndrome that arises predominantly from germline phosphatase and tensin homologue deleted on chromosome 10 (PTEN) mutation and increased phosphoinositide 3-kinase/mammalian target of rapamycin (PI3K/mTOR) signalling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP741798.RA7RO3xQlD543-Wi9Guo3wupEUveSQUukrgb0UPC9JsCg130_provenance.
- NP741798.RA7RO3xQlD543-Wi9Guo3wupEUveSQUukrgb0UPC9JsCg130_assertion evidence source_evidence_literature NP741798.RA7RO3xQlD543-Wi9Guo3wupEUveSQUukrgb0UPC9JsCg130_provenance.
- NP741798.RA7RO3xQlD543-Wi9Guo3wupEUveSQUukrgb0UPC9JsCg130_assertion SIO_000772 21361912 NP741798.RA7RO3xQlD543-Wi9Guo3wupEUveSQUukrgb0UPC9JsCg130_provenance.
- NP741798.RA7RO3xQlD543-Wi9Guo3wupEUveSQUukrgb0UPC9JsCg130_assertion wasDerivedFrom befree-20140225 NP741798.RA7RO3xQlD543-Wi9Guo3wupEUveSQUukrgb0UPC9JsCg130_provenance.
- NP741798.RA7RO3xQlD543-Wi9Guo3wupEUveSQUukrgb0UPC9JsCg130_assertion wasGeneratedBy ECO_0000203 NP741798.RA7RO3xQlD543-Wi9Guo3wupEUveSQUukrgb0UPC9JsCg130_provenance.