Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP624836.RAXdJnGXC0pdPTPLMGKRP7l7WKvl-3UklHgWMydQtRmE4130_assertion> ?p ?o ?g. }
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- NP624836.RAXdJnGXC0pdPTPLMGKRP7l7WKvl-3UklHgWMydQtRmE4130_assertion type Assertion NP624836.RAXdJnGXC0pdPTPLMGKRP7l7WKvl-3UklHgWMydQtRmE4130_head.
- NP624836.RAXdJnGXC0pdPTPLMGKRP7l7WKvl-3UklHgWMydQtRmE4130_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." NP624836.RAXdJnGXC0pdPTPLMGKRP7l7WKvl-3UklHgWMydQtRmE4130_provenance.
- NP624836.RAXdJnGXC0pdPTPLMGKRP7l7WKvl-3UklHgWMydQtRmE4130_assertion evidence source_evidence_literature NP624836.RAXdJnGXC0pdPTPLMGKRP7l7WKvl-3UklHgWMydQtRmE4130_provenance.
- NP624836.RAXdJnGXC0pdPTPLMGKRP7l7WKvl-3UklHgWMydQtRmE4130_assertion SIO_000772 21361912 NP624836.RAXdJnGXC0pdPTPLMGKRP7l7WKvl-3UklHgWMydQtRmE4130_provenance.
- NP624836.RAXdJnGXC0pdPTPLMGKRP7l7WKvl-3UklHgWMydQtRmE4130_assertion wasDerivedFrom befree-20150227 NP624836.RAXdJnGXC0pdPTPLMGKRP7l7WKvl-3UklHgWMydQtRmE4130_provenance.
- NP624836.RAXdJnGXC0pdPTPLMGKRP7l7WKvl-3UklHgWMydQtRmE4130_assertion wasGeneratedBy ECO_0000203 NP624836.RAXdJnGXC0pdPTPLMGKRP7l7WKvl-3UklHgWMydQtRmE4130_provenance.