Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP294158.RAFYYKHE5rpI_c2kMofSnmRpnzWIKnG9yiOLmmzefmJuY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP294158.RAFYYKHE5rpI_c2kMofSnmRpnzWIKnG9yiOLmmzefmJuY130_assertion type Assertion NP294158.RAFYYKHE5rpI_c2kMofSnmRpnzWIKnG9yiOLmmzefmJuY130_head.
- NP294158.RAFYYKHE5rpI_c2kMofSnmRpnzWIKnG9yiOLmmzefmJuY130_assertion description "[We conclude that germline mutations in PRKAR1A, an apparent tumour-suppressor gene, are responsible for the CNC phenotype in a subset of patients with this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294158.RAFYYKHE5rpI_c2kMofSnmRpnzWIKnG9yiOLmmzefmJuY130_provenance.
- NP294158.RAFYYKHE5rpI_c2kMofSnmRpnzWIKnG9yiOLmmzefmJuY130_assertion evidence source_evidence_literature NP294158.RAFYYKHE5rpI_c2kMofSnmRpnzWIKnG9yiOLmmzefmJuY130_provenance.
- NP294158.RAFYYKHE5rpI_c2kMofSnmRpnzWIKnG9yiOLmmzefmJuY130_assertion SIO_000772 10973256 NP294158.RAFYYKHE5rpI_c2kMofSnmRpnzWIKnG9yiOLmmzefmJuY130_provenance.
- NP294158.RAFYYKHE5rpI_c2kMofSnmRpnzWIKnG9yiOLmmzefmJuY130_assertion wasDerivedFrom befree-2016 NP294158.RAFYYKHE5rpI_c2kMofSnmRpnzWIKnG9yiOLmmzefmJuY130_provenance.
- NP294158.RAFYYKHE5rpI_c2kMofSnmRpnzWIKnG9yiOLmmzefmJuY130_assertion wasGeneratedBy ECO_0000203 NP294158.RAFYYKHE5rpI_c2kMofSnmRpnzWIKnG9yiOLmmzefmJuY130_provenance.