Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP527854.RATSxYMr0h5hjTs9zk4BAMQvc0O51B5QYuAOpdvDEDo2g130_assertion> ?p ?o ?g. }
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- NP527854.RATSxYMr0h5hjTs9zk4BAMQvc0O51B5QYuAOpdvDEDo2g130_assertion type Assertion NP527854.RATSxYMr0h5hjTs9zk4BAMQvc0O51B5QYuAOpdvDEDo2g130_head.
- NP527854.RATSxYMr0h5hjTs9zk4BAMQvc0O51B5QYuAOpdvDEDo2g130_assertion wasGeneratedBy ECO_0000203 NP527854.RATSxYMr0h5hjTs9zk4BAMQvc0O51B5QYuAOpdvDEDo2g130_provenance.
- NP527854.RATSxYMr0h5hjTs9zk4BAMQvc0O51B5QYuAOpdvDEDo2g130_assertion wasDerivedFrom befree-20150227 NP527854.RATSxYMr0h5hjTs9zk4BAMQvc0O51B5QYuAOpdvDEDo2g130_provenance.
- NP527854.RATSxYMr0h5hjTs9zk4BAMQvc0O51B5QYuAOpdvDEDo2g130_assertion SIO_000772 17468812 NP527854.RATSxYMr0h5hjTs9zk4BAMQvc0O51B5QYuAOpdvDEDo2g130_provenance.
- NP527854.RATSxYMr0h5hjTs9zk4BAMQvc0O51B5QYuAOpdvDEDo2g130_assertion evidence source_evidence_literature NP527854.RATSxYMr0h5hjTs9zk4BAMQvc0O51B5QYuAOpdvDEDo2g130_provenance.
- NP527854.RATSxYMr0h5hjTs9zk4BAMQvc0O51B5QYuAOpdvDEDo2g130_assertion description "[We report on a novel KRAS gene mutation in a patient presenting the clinical features typical of Costello syndrome and the additional findings seen in Noonan syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527854.RATSxYMr0h5hjTs9zk4BAMQvc0O51B5QYuAOpdvDEDo2g130_provenance.