Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_provenance.
- NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_assertion wasGeneratedBy ECO_0000203 NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_provenance.
- NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_assertion wasDerivedFrom befree-20140225 NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_provenance.
- NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_assertion SIO_000772 10394936 NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_provenance.
- NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_assertion evidence source_evidence_literature NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_provenance.
- NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_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." NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_provenance.