Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP526678.RAzwEOQ5MP0X18GbpddWCT6I4NeA_V8U3YGOPwUp6mCdU130_assertion> ?p ?o ?g. }
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- NP526678.RAzwEOQ5MP0X18GbpddWCT6I4NeA_V8U3YGOPwUp6mCdU130_assertion type Assertion NP526678.RAzwEOQ5MP0X18GbpddWCT6I4NeA_V8U3YGOPwUp6mCdU130_head.
- NP526678.RAzwEOQ5MP0X18GbpddWCT6I4NeA_V8U3YGOPwUp6mCdU130_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." NP526678.RAzwEOQ5MP0X18GbpddWCT6I4NeA_V8U3YGOPwUp6mCdU130_provenance.
- NP526678.RAzwEOQ5MP0X18GbpddWCT6I4NeA_V8U3YGOPwUp6mCdU130_assertion evidence source_evidence_literature NP526678.RAzwEOQ5MP0X18GbpddWCT6I4NeA_V8U3YGOPwUp6mCdU130_provenance.
- NP526678.RAzwEOQ5MP0X18GbpddWCT6I4NeA_V8U3YGOPwUp6mCdU130_assertion SIO_000772 21361912 NP526678.RAzwEOQ5MP0X18GbpddWCT6I4NeA_V8U3YGOPwUp6mCdU130_provenance.
- NP526678.RAzwEOQ5MP0X18GbpddWCT6I4NeA_V8U3YGOPwUp6mCdU130_assertion wasDerivedFrom befree-20140225 NP526678.RAzwEOQ5MP0X18GbpddWCT6I4NeA_V8U3YGOPwUp6mCdU130_provenance.
- NP526678.RAzwEOQ5MP0X18GbpddWCT6I4NeA_V8U3YGOPwUp6mCdU130_assertion wasGeneratedBy ECO_0000203 NP526678.RAzwEOQ5MP0X18GbpddWCT6I4NeA_V8U3YGOPwUp6mCdU130_provenance.