Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_assertion> ?p ?o ?g. }
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- NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_assertion type Assertion NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_head.
- NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_assertion wasGeneratedBy ECO_0000203 NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_provenance.
- NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_assertion wasDerivedFrom befree-20150227 NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_provenance.
- NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_assertion SIO_000772 10394936 NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_provenance.
- NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_assertion evidence source_evidence_literature NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_provenance.
- NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_assertion description "[Pfeiffer syndrome (PS) is one of the classical craniosynostosis syndromes correlated with specific mutations in the human fibroblast growth factor receptor (FGFR) genes, FGFR1 and FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_provenance.