Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP852217.RALifQ9ZoQ_T_yoAqTYKB-YtBT4HUhEa_MgP6tnljTf8o130_assertion> ?p ?o ?g. }
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- NP852217.RALifQ9ZoQ_T_yoAqTYKB-YtBT4HUhEa_MgP6tnljTf8o130_assertion type Assertion NP852217.RALifQ9ZoQ_T_yoAqTYKB-YtBT4HUhEa_MgP6tnljTf8o130_head.
- NP852217.RALifQ9ZoQ_T_yoAqTYKB-YtBT4HUhEa_MgP6tnljTf8o130_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." NP852217.RALifQ9ZoQ_T_yoAqTYKB-YtBT4HUhEa_MgP6tnljTf8o130_provenance.
- NP852217.RALifQ9ZoQ_T_yoAqTYKB-YtBT4HUhEa_MgP6tnljTf8o130_assertion evidence source_evidence_literature NP852217.RALifQ9ZoQ_T_yoAqTYKB-YtBT4HUhEa_MgP6tnljTf8o130_provenance.
- NP852217.RALifQ9ZoQ_T_yoAqTYKB-YtBT4HUhEa_MgP6tnljTf8o130_assertion SIO_000772 21361912 NP852217.RALifQ9ZoQ_T_yoAqTYKB-YtBT4HUhEa_MgP6tnljTf8o130_provenance.
- NP852217.RALifQ9ZoQ_T_yoAqTYKB-YtBT4HUhEa_MgP6tnljTf8o130_assertion wasDerivedFrom befree-20140225 NP852217.RALifQ9ZoQ_T_yoAqTYKB-YtBT4HUhEa_MgP6tnljTf8o130_provenance.
- NP852217.RALifQ9ZoQ_T_yoAqTYKB-YtBT4HUhEa_MgP6tnljTf8o130_assertion wasGeneratedBy ECO_0000203 NP852217.RALifQ9ZoQ_T_yoAqTYKB-YtBT4HUhEa_MgP6tnljTf8o130_provenance.