Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_assertion> ?p ?o ?g. }
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- NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_assertion type Assertion NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_head.
- NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_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." NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_provenance.
- NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_assertion evidence source_evidence_literature NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_provenance.
- NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_assertion SIO_000772 21082653 NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_provenance.
- NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_assertion wasDerivedFrom befree-2016 NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_provenance.
- NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_assertion wasGeneratedBy ECO_0000203 NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_provenance.