Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP412280.RAKpH6daqgNusiYgcEubSg0rxdTeflFV-j3C5SgudagTI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP412280.RAKpH6daqgNusiYgcEubSg0rxdTeflFV-j3C5SgudagTI130_assertion type Assertion NP412280.RAKpH6daqgNusiYgcEubSg0rxdTeflFV-j3C5SgudagTI130_head.
- NP412280.RAKpH6daqgNusiYgcEubSg0rxdTeflFV-j3C5SgudagTI130_assertion description "[Clinical review of known individuals with MEK1/MEK2 mutations suggests that these patients show dysmorphic features, ectodermal abnormalities and cognitive deficit similar to what was observed in BRAF-mutated patients and in the general CFCS population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412280.RAKpH6daqgNusiYgcEubSg0rxdTeflFV-j3C5SgudagTI130_provenance.
- NP412280.RAKpH6daqgNusiYgcEubSg0rxdTeflFV-j3C5SgudagTI130_assertion evidence source_evidence_literature NP412280.RAKpH6daqgNusiYgcEubSg0rxdTeflFV-j3C5SgudagTI130_provenance.
- NP412280.RAKpH6daqgNusiYgcEubSg0rxdTeflFV-j3C5SgudagTI130_assertion SIO_000772 19156172 NP412280.RAKpH6daqgNusiYgcEubSg0rxdTeflFV-j3C5SgudagTI130_provenance.
- NP412280.RAKpH6daqgNusiYgcEubSg0rxdTeflFV-j3C5SgudagTI130_assertion wasDerivedFrom befree-20140225 NP412280.RAKpH6daqgNusiYgcEubSg0rxdTeflFV-j3C5SgudagTI130_provenance.
- NP412280.RAKpH6daqgNusiYgcEubSg0rxdTeflFV-j3C5SgudagTI130_assertion wasGeneratedBy ECO_0000203 NP412280.RAKpH6daqgNusiYgcEubSg0rxdTeflFV-j3C5SgudagTI130_provenance.