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- B052b4633abf1e2989d0b0c37c0f8479a hasDbXref "DOID:0060856" @default.
- B052b4633abf1e2989d0b0c37c0f8479a hasDbXref "PMID:14648004" @default.
- B052b4633abf1e2989d0b0c37c0f8479a hasDbXref "PMID:20413652" @default.
- B052b4633abf1e2989d0b0c37c0f8479a type Axiom @default.
- B052b4633abf1e2989d0b0c37c0f8479a annotatedProperty IAO_0000115 @default.
- B052b4633abf1e2989d0b0c37c0f8479a annotatedSource MONDO_0008832 @default.
- B052b4633abf1e2989d0b0c37c0f8479a annotatedTarget "A visceral heterotaxy characterized by complete atrioventricular septal defect with a common atrium and univentricular AV connection, total anomalous pulmonary drainage, and transposition or malposition of the great arteries and may be associated with bilateral trilobed lungs, midline liver, asplenia and situs inversus affecting other organs that has material basis in homozygous mutation in the GDF1 gene on chromosome 19p12." @default.