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Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C51543> ?p ?o ?g. }

• NCIT_C51543 IAO_0000115 "Human FGFR2 wild-type allele is located within 10q26 and is approximately 875 kb in length. This allele, which encodes fibroblast growth factor receptor 2 protein, plays a role in mitogenesis and differentiation by mediating the binding interactions of keratinocyte growth factor. Mutations in the gene are associated with Crouzon syndrome, Pfeiffer syndrome, Craniosynostosis, Apert syndrome, Jackson-Weiss syndrome, Beare-Stevenson cutis gyrata syndrome, Saethre-Chotzen syndrome, and syndromic craniosynostosis." @default.
• NCIT_C51543 NCIT_NHC0 "C51543" @default.
• NCIT_C51543 NCIT_P100 "176943" @default.
• NCIT_C51543 NCIT_P101 "FGFR Family, Bek (Mouse), bFGFR (Chicken)" @default.
• NCIT_C51543 NCIT_P102 "NM_000141" @default.
• NCIT_C51543 NCIT_P106 "Gene or Genome" @default.
• NCIT_C51543 NCIT_P107 "FGFR2 wt Allele" @default.
• NCIT_C51543 NCIT_P108 "FGFR2 wt Allele" @default.
• NCIT_C51543 NCIT_P171 "17529967 and 17529973" @default.
• NCIT_C51543 NCIT_P207 "C1704724" @default.
• NCIT_C51543 NCIT_P211 "fibroblast growth factor receptor activity" @default.
• NCIT_C51543 NCIT_P211 "integral to membrane" @default.
• NCIT_C51543 NCIT_P211 "protein amino acid phosphorylation" @default.
• NCIT_C51543 NCIT_P211 "protein tyrosine kinase activity" @default.
• NCIT_C51543 NCIT_P321 "2263" @default.
• NCIT_C51543 NCIT_P322 "CTRP" @default.
• NCIT_C51543 NCIT_P366 "FGFR2_wt_Allele" @default.
• NCIT_C51543 NCIT_P96 "Fibroblast Growth Factor Receptor 2" @default.
• NCIT_C51543 NCIT_P98 "Five SNPs for the FGFR2 gene (rs2981582, rs11200014, rs2981579, rs1219648 and rs2420946) have been linked to increased breast cancer incidence. (Nature Genetics 2007; 39:870-874 and Nature 2007; 447:1087-1093)" @default.
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