Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_assertion type Assertion NP399857.RAEIQjDLke4iduMyzhWwjm38DGloP5pPQH5FloUW5puZ0130_head.
- 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.