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- NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_assertion type Assertion NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_head.
- NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_assertion wasGeneratedBy ECO_0000203 NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_provenance.
- NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_assertion wasDerivedFrom befree-2016 NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_provenance.
- NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_assertion SIO_000772 11055896 NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_provenance.
- NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_assertion evidence source_evidence_literature NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_provenance.
- NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_assertion description "[Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_provenance.