Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_provenance.
- NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_assertion description "[The mutations in Pfeiffer (FGFR1), Muenke (FGFR3), and Apert syndrome (FGFR2) are caused by the same amino acid substitution in a highly conserved region of the Ig II-III linker region of these proteins, which suggests that these receptor tyrosine kinases have an overlapping function in suture biology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_provenance.
- NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_assertion evidence source_evidence_literature NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_provenance.
- NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_assertion SIO_000772 17552943 NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_provenance.
- NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_assertion wasDerivedFrom befree-20150227 NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_provenance.
- NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_assertion wasGeneratedBy ECO_0000203 NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP400145.RAROFLivGWbBd5JMa58JizGBUnCI5t3xZ5-y0ddCw0ICQ130_provenance.