Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the 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.
- NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_assertion evidence source_evidence_literature NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_provenance.
- NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_assertion SIO_000772 11055896 NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_provenance.
- NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_assertion wasDerivedFrom befree-2016 NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_provenance.
- NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_assertion wasGeneratedBy ECO_0000203 NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_provenance.
- befree-2016 importedOn "2016-02-19" NP298858.RASwdohOl3uRusJUbNqL3QY6WgtQLxKCEOt0k2IvJ_VjE130_provenance.