Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B970194eae5ab7a03d55f6cf95f7382f6> ?p ?o ?g. }
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- B970194eae5ab7a03d55f6cf95f7382f6 hasDbXref "DOID:0050600" @default.
- B970194eae5ab7a03d55f6cf95f7382f6 hasDbXref "OMIM:600501" @default.
- B970194eae5ab7a03d55f6cf95f7382f6 hasDbXref "http://en.wikipedia.org/wiki/ABCD_syndrome" @default.
- B970194eae5ab7a03d55f6cf95f7382f6 type Axiom @default.
- B970194eae5ab7a03d55f6cf95f7382f6 annotatedProperty IAO_0000115 @default.
- B970194eae5ab7a03d55f6cf95f7382f6 annotatedSource MONDO_0010895 @default.
- B970194eae5ab7a03d55f6cf95f7382f6 annotatedTarget "An autosomal recessive disease that is characterized by albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness and has material basis in a mutation in the endothelin B receptor gene (EDNRB)." @default.