Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_assertion> ?p ?o ?g. }
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- NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_assertion type Assertion NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_head.
- NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_provenance.
- NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_assertion evidence source_evidence_literature NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_provenance.
- NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_assertion SIO_000772 21082653 NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_provenance.
- NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_assertion wasDerivedFrom befree-20140225 NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_provenance.
- NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_assertion wasGeneratedBy ECO_0000203 NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_provenance.