Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_assertion> ?p ?o ?g. }
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- NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_assertion type Assertion NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_head.
- NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_assertion description "[Muenke syndrome is an autosomal dominant craniosynostosis syndrome resulting from a defining point mutation in the Fibroblast Growth Factor Receptor3 (FGFR3) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_provenance.
- NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_assertion evidence source_evidence_literature NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_provenance.
- NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_assertion SIO_000772 23378035 NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_provenance.
- NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_assertion wasDerivedFrom befree-20140225 NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_provenance.
- NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_assertion wasGeneratedBy ECO_0000203 NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_provenance.