Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C51725> ?p ?o ?g. }
- NCIT_C51725 IAO_0000115 "Human ACVRL1 wild-type allele is located within 12q11-q14 and is approximately 14 kb in length. This allele, which encodes serine/threonine-protein kinase receptor R3 protein, is involved in receptor signal transduction. ACVRL1 deficiency causes hemorrhagic telangiectasia type 2, which is also also known as Rendu-Osler-Weber syndrome 2." @default.
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- NCIT_C51725 NCIT_P211 "circulation" @default.
- NCIT_C51725 NCIT_P211 "integral to plasma membrane" @default.
- NCIT_C51725 NCIT_P211 "transmembrane receptor protein serine/threonine kinase activity" @default.
- NCIT_C51725 NCIT_P321 "94" @default.
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- NCIT_C51725 hasExactSynonym "ACVRL1 wt Allele" @default.
- NCIT_C51725 hasExactSynonym "ACVRL1" @default.
- NCIT_C51725 hasExactSynonym "ACVRLK1" @default.
- NCIT_C51725 hasExactSynonym "ALK-1" @default.
- NCIT_C51725 hasExactSynonym "ALK1" @default.
- NCIT_C51725 hasExactSynonym "Activin A Receptor, Type II-Like Kinase 1 wt Allele" @default.
- NCIT_C51725 hasExactSynonym "Activin Receptor-Like Kinase 1 Gene" @default.
- NCIT_C51725 hasExactSynonym "HHT" @default.
- NCIT_C51725 hasExactSynonym "HHT2" @default.
- NCIT_C51725 hasExactSynonym "ORW2" @default.
- NCIT_C51725 hasExactSynonym "SKR3" @default.
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- NCIT_C51725 label "ACVRL1 wt Allele" @default.
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