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- NP907661.RAwekuKzAsabNeoMcbo3av3p20874i4bjtQNpNjhsW9Sg130_assertion type Assertion NP907661.RAwekuKzAsabNeoMcbo3av3p20874i4bjtQNpNjhsW9Sg130_head.
- NP907661.RAwekuKzAsabNeoMcbo3av3p20874i4bjtQNpNjhsW9Sg130_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." NP907661.RAwekuKzAsabNeoMcbo3av3p20874i4bjtQNpNjhsW9Sg130_provenance.
- NP907661.RAwekuKzAsabNeoMcbo3av3p20874i4bjtQNpNjhsW9Sg130_assertion evidence source_evidence_literature NP907661.RAwekuKzAsabNeoMcbo3av3p20874i4bjtQNpNjhsW9Sg130_provenance.
- NP907661.RAwekuKzAsabNeoMcbo3av3p20874i4bjtQNpNjhsW9Sg130_assertion SIO_000772 21082653 NP907661.RAwekuKzAsabNeoMcbo3av3p20874i4bjtQNpNjhsW9Sg130_provenance.
- NP907661.RAwekuKzAsabNeoMcbo3av3p20874i4bjtQNpNjhsW9Sg130_assertion wasDerivedFrom befree-20150227 NP907661.RAwekuKzAsabNeoMcbo3av3p20874i4bjtQNpNjhsW9Sg130_provenance.
- NP907661.RAwekuKzAsabNeoMcbo3av3p20874i4bjtQNpNjhsW9Sg130_assertion wasGeneratedBy ECO_0000203 NP907661.RAwekuKzAsabNeoMcbo3av3p20874i4bjtQNpNjhsW9Sg130_provenance.