Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_provenance.
- NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_assertion description "[However, unlike the Apert syndrome Pro253Arg FGFR2c mutant, neither the Pfeiffer syndrome Pro250Arg FGFR1c mutant nor the Muenke syndrome Pro250Arg FGFR3c mutant bound appreciably to FGF7 or FGF10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_provenance.
- NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_assertion evidence source_evidence_literature NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_provenance.
- NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_assertion SIO_000772 14613973 NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_provenance.
- NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_assertion wasDerivedFrom befree-20150227 NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_provenance.
- NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_assertion wasGeneratedBy ECO_0000203 NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_provenance.