Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_provenance.
- 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.