Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP420426.RA0ywxFyFmJCmhV1fwuNlwKMaL2dLTw8y-lawYV1I3T6g130_assertion> ?p ?o ?g. }
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- NP420426.RA0ywxFyFmJCmhV1fwuNlwKMaL2dLTw8y-lawYV1I3T6g130_assertion type Assertion NP420426.RA0ywxFyFmJCmhV1fwuNlwKMaL2dLTw8y-lawYV1I3T6g130_head.
- NP420426.RA0ywxFyFmJCmhV1fwuNlwKMaL2dLTw8y-lawYV1I3T6g130_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." NP420426.RA0ywxFyFmJCmhV1fwuNlwKMaL2dLTw8y-lawYV1I3T6g130_provenance.
- NP420426.RA0ywxFyFmJCmhV1fwuNlwKMaL2dLTw8y-lawYV1I3T6g130_assertion evidence source_evidence_literature NP420426.RA0ywxFyFmJCmhV1fwuNlwKMaL2dLTw8y-lawYV1I3T6g130_provenance.
- NP420426.RA0ywxFyFmJCmhV1fwuNlwKMaL2dLTw8y-lawYV1I3T6g130_assertion SIO_000772 14613973 NP420426.RA0ywxFyFmJCmhV1fwuNlwKMaL2dLTw8y-lawYV1I3T6g130_provenance.
- NP420426.RA0ywxFyFmJCmhV1fwuNlwKMaL2dLTw8y-lawYV1I3T6g130_assertion wasDerivedFrom befree-2016 NP420426.RA0ywxFyFmJCmhV1fwuNlwKMaL2dLTw8y-lawYV1I3T6g130_provenance.
- NP420426.RA0ywxFyFmJCmhV1fwuNlwKMaL2dLTw8y-lawYV1I3T6g130_assertion wasGeneratedBy ECO_0000203 NP420426.RA0ywxFyFmJCmhV1fwuNlwKMaL2dLTw8y-lawYV1I3T6g130_provenance.