Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP401475.RAZrSHfstLTuWTrbT7tihx58DaRUg-gYSlQ0EwZ1oYXTo130_assertion> ?p ?o ?g. }
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- NP401475.RAZrSHfstLTuWTrbT7tihx58DaRUg-gYSlQ0EwZ1oYXTo130_assertion type Assertion NP401475.RAZrSHfstLTuWTrbT7tihx58DaRUg-gYSlQ0EwZ1oYXTo130_head.
- NP401475.RAZrSHfstLTuWTrbT7tihx58DaRUg-gYSlQ0EwZ1oYXTo130_assertion description "[Here we investigate growth of the skull in two inbred mouse models each carrying one of two gain-of-function mutations in FGFR2 on neighboring amino acids (S252W and P253R) that in humans cause Apert syndrome, one of the most severe FGFR-related craniosynostosis syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401475.RAZrSHfstLTuWTrbT7tihx58DaRUg-gYSlQ0EwZ1oYXTo130_provenance.
- NP401475.RAZrSHfstLTuWTrbT7tihx58DaRUg-gYSlQ0EwZ1oYXTo130_assertion evidence source_evidence_literature NP401475.RAZrSHfstLTuWTrbT7tihx58DaRUg-gYSlQ0EwZ1oYXTo130_provenance.
- NP401475.RAZrSHfstLTuWTrbT7tihx58DaRUg-gYSlQ0EwZ1oYXTo130_assertion SIO_000772 24580805 NP401475.RAZrSHfstLTuWTrbT7tihx58DaRUg-gYSlQ0EwZ1oYXTo130_provenance.
- NP401475.RAZrSHfstLTuWTrbT7tihx58DaRUg-gYSlQ0EwZ1oYXTo130_assertion wasDerivedFrom befree-20150227 NP401475.RAZrSHfstLTuWTrbT7tihx58DaRUg-gYSlQ0EwZ1oYXTo130_provenance.
- NP401475.RAZrSHfstLTuWTrbT7tihx58DaRUg-gYSlQ0EwZ1oYXTo130_assertion wasGeneratedBy ECO_0000203 NP401475.RAZrSHfstLTuWTrbT7tihx58DaRUg-gYSlQ0EwZ1oYXTo130_provenance.