Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP722542.RAnXXcjXWgvgHhpPu_-cFphSZghsAmqXQSWDmbER7AcO8130_assertion> ?p ?o ?g. }
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- NP722542.RAnXXcjXWgvgHhpPu_-cFphSZghsAmqXQSWDmbER7AcO8130_assertion type Assertion NP722542.RAnXXcjXWgvgHhpPu_-cFphSZghsAmqXQSWDmbER7AcO8130_head.
- NP722542.RAnXXcjXWgvgHhpPu_-cFphSZghsAmqXQSWDmbER7AcO8130_assertion wasGeneratedBy ECO_0000203 NP722542.RAnXXcjXWgvgHhpPu_-cFphSZghsAmqXQSWDmbER7AcO8130_provenance.
- NP722542.RAnXXcjXWgvgHhpPu_-cFphSZghsAmqXQSWDmbER7AcO8130_assertion wasDerivedFrom befree-2016 NP722542.RAnXXcjXWgvgHhpPu_-cFphSZghsAmqXQSWDmbER7AcO8130_provenance.
- NP722542.RAnXXcjXWgvgHhpPu_-cFphSZghsAmqXQSWDmbER7AcO8130_assertion SIO_000772 19243295 NP722542.RAnXXcjXWgvgHhpPu_-cFphSZghsAmqXQSWDmbER7AcO8130_provenance.
- NP722542.RAnXXcjXWgvgHhpPu_-cFphSZghsAmqXQSWDmbER7AcO8130_assertion evidence source_evidence_literature NP722542.RAnXXcjXWgvgHhpPu_-cFphSZghsAmqXQSWDmbER7AcO8130_provenance.
- NP722542.RAnXXcjXWgvgHhpPu_-cFphSZghsAmqXQSWDmbER7AcO8130_assertion description "[The majority of the mutations identified are identical to germline mutations in FGFR2 and FGFR3 that cause craniosynostosis and hypochondroplasia syndromes and result in both ligand-independent and ligand-dependent receptor activation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722542.RAnXXcjXWgvgHhpPu_-cFphSZghsAmqXQSWDmbER7AcO8130_provenance.