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<http://identifiers.org/ensembl/ENSG00000132932> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16612> <http://purl.org/np/RAS1YLKTHh7T7ciTH0U-zSoBIsXh2a93eWkySVA1OqNhc#assertion> .
<http://identifiers.org/ensembl/ENSG00000132932> <http://www.w3.org/2000/01/rdf-schema#label> "ATP8A2" <http://purl.org/np/RAS1YLKTHh7T7ciTH0U-zSoBIsXh2a93eWkySVA1OqNhc#assertion> .
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<http://identifiers.org/pubmed/22892528> <http://purl.org/dc/terms/title> "Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion." <http://purl.org/np/RAS1YLKTHh7T7ciTH0U-zSoBIsXh2a93eWkySVA1OqNhc#provenance> .
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