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- NP414207.RAIeVw8Hg3UghYa_QplgYSNSzGHCBKhbe_24Fpqp3Ngc0130_assertion type Assertion NP414207.RAIeVw8Hg3UghYa_QplgYSNSzGHCBKhbe_24Fpqp3Ngc0130_head.
- NP414207.RAIeVw8Hg3UghYa_QplgYSNSzGHCBKhbe_24Fpqp3Ngc0130_assertion wasGeneratedBy ECO_0000203 NP414207.RAIeVw8Hg3UghYa_QplgYSNSzGHCBKhbe_24Fpqp3Ngc0130_provenance.
- NP414207.RAIeVw8Hg3UghYa_QplgYSNSzGHCBKhbe_24Fpqp3Ngc0130_assertion wasDerivedFrom befree-2016 NP414207.RAIeVw8Hg3UghYa_QplgYSNSzGHCBKhbe_24Fpqp3Ngc0130_provenance.
- NP414207.RAIeVw8Hg3UghYa_QplgYSNSzGHCBKhbe_24Fpqp3Ngc0130_assertion SIO_000772 14506070 NP414207.RAIeVw8Hg3UghYa_QplgYSNSzGHCBKhbe_24Fpqp3Ngc0130_provenance.
- NP414207.RAIeVw8Hg3UghYa_QplgYSNSzGHCBKhbe_24Fpqp3Ngc0130_assertion evidence source_evidence_literature NP414207.RAIeVw8Hg3UghYa_QplgYSNSzGHCBKhbe_24Fpqp3Ngc0130_provenance.
- NP414207.RAIeVw8Hg3UghYa_QplgYSNSzGHCBKhbe_24Fpqp3Ngc0130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414207.RAIeVw8Hg3UghYa_QplgYSNSzGHCBKhbe_24Fpqp3Ngc0130_provenance.