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- NP1215494.RAZDTKVoGJwTnd4JLay5qeDiw6pJ8sq-V3NJ3NEX-x_G4130_assertion type Assertion NP1215494.RAZDTKVoGJwTnd4JLay5qeDiw6pJ8sq-V3NJ3NEX-x_G4130_head.
- NP1215494.RAZDTKVoGJwTnd4JLay5qeDiw6pJ8sq-V3NJ3NEX-x_G4130_assertion description "[We provide experimental evidence that these mutations affect normal FGFR2 splicing and document the clinical consequences, which include a mild Crouzon syndrome phenotype and reduced penetrance of craniosynostosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215494.RAZDTKVoGJwTnd4JLay5qeDiw6pJ8sq-V3NJ3NEX-x_G4130_provenance.
- NP1215494.RAZDTKVoGJwTnd4JLay5qeDiw6pJ8sq-V3NJ3NEX-x_G4130_assertion evidence source_evidence_literature NP1215494.RAZDTKVoGJwTnd4JLay5qeDiw6pJ8sq-V3NJ3NEX-x_G4130_provenance.
- NP1215494.RAZDTKVoGJwTnd4JLay5qeDiw6pJ8sq-V3NJ3NEX-x_G4130_assertion SIO_000772 25174698 NP1215494.RAZDTKVoGJwTnd4JLay5qeDiw6pJ8sq-V3NJ3NEX-x_G4130_provenance.
- NP1215494.RAZDTKVoGJwTnd4JLay5qeDiw6pJ8sq-V3NJ3NEX-x_G4130_assertion wasDerivedFrom befree-2016 NP1215494.RAZDTKVoGJwTnd4JLay5qeDiw6pJ8sq-V3NJ3NEX-x_G4130_provenance.
- NP1215494.RAZDTKVoGJwTnd4JLay5qeDiw6pJ8sq-V3NJ3NEX-x_G4130_assertion wasGeneratedBy ECO_0000203 NP1215494.RAZDTKVoGJwTnd4JLay5qeDiw6pJ8sq-V3NJ3NEX-x_G4130_provenance.