Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP646022.RA6RmXPdPjMzTnn4QRFDSx0tN77xy-9QqTHXL43JTB0gM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP646022.RA6RmXPdPjMzTnn4QRFDSx0tN77xy-9QqTHXL43JTB0gM130_assertion type Assertion NP646022.RA6RmXPdPjMzTnn4QRFDSx0tN77xy-9QqTHXL43JTB0gM130_head.
- NP646022.RA6RmXPdPjMzTnn4QRFDSx0tN77xy-9QqTHXL43JTB0gM130_assertion description "[Mutational analysis of the affected MEK1 and MEK2 exons did not reveal occurrence of mutations among 75 patients with Noonan syndrome, confirming the low prevalence of MEK gene defects in this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP646022.RA6RmXPdPjMzTnn4QRFDSx0tN77xy-9QqTHXL43JTB0gM130_provenance.
- NP646022.RA6RmXPdPjMzTnn4QRFDSx0tN77xy-9QqTHXL43JTB0gM130_assertion evidence source_evidence_literature NP646022.RA6RmXPdPjMzTnn4QRFDSx0tN77xy-9QqTHXL43JTB0gM130_provenance.
- NP646022.RA6RmXPdPjMzTnn4QRFDSx0tN77xy-9QqTHXL43JTB0gM130_assertion SIO_000772 19156172 NP646022.RA6RmXPdPjMzTnn4QRFDSx0tN77xy-9QqTHXL43JTB0gM130_provenance.
- NP646022.RA6RmXPdPjMzTnn4QRFDSx0tN77xy-9QqTHXL43JTB0gM130_assertion wasDerivedFrom befree-20150227 NP646022.RA6RmXPdPjMzTnn4QRFDSx0tN77xy-9QqTHXL43JTB0gM130_provenance.
- NP646022.RA6RmXPdPjMzTnn4QRFDSx0tN77xy-9QqTHXL43JTB0gM130_assertion wasGeneratedBy ECO_0000203 NP646022.RA6RmXPdPjMzTnn4QRFDSx0tN77xy-9QqTHXL43JTB0gM130_provenance.