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<http://purl.org/np/RAuCkR_W8_jbTlpDJ-_lzcVfyLZdHhq5l6SpN2iMEE3as> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#Nanopublication> <http://purl.org/np/RAuCkR_W8_jbTlpDJ-_lzcVfyLZdHhq5l6SpN2iMEE3as#head> .
<http://identifiers.org/ensembl/ENSG00000152208> <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/RAuCkR_W8_jbTlpDJ-_lzcVfyLZdHhq5l6SpN2iMEE3as#assertion> .
<http://identifiers.org/ensembl/ENSG00000152208> <http://www.w3.org/2000/01/rdf-schema#label> "GRID2" <http://purl.org/np/RAuCkR_W8_jbTlpDJ-_lzcVfyLZdHhq5l6SpN2iMEE3as#assertion> .
<http://purl.org/np/RAuCkR_W8_jbTlpDJ-_lzcVfyLZdHhq5l6SpN2iMEE3as#association> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ensembl/ENSG00000152208> <http://purl.org/np/RAuCkR_W8_jbTlpDJ-_lzcVfyLZdHhq5l6SpN2iMEE3as#assertion> .
<http://purl.org/np/RAuCkR_W8_jbTlpDJ-_lzcVfyLZdHhq5l6SpN2iMEE3as#association> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/omim/616204> <http://purl.org/np/RAuCkR_W8_jbTlpDJ-_lzcVfyLZdHhq5l6SpN2iMEE3as#assertion> .
<http://purl.org/np/RAuCkR_W8_jbTlpDJ-_lzcVfyLZdHhq5l6SpN2iMEE3as#association> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_000983> <http://purl.org/np/RAuCkR_W8_jbTlpDJ-_lzcVfyLZdHhq5l6SpN2iMEE3as#assertion> .
<http://identifiers.org/pubmed/23611888> <http://purl.org/dc/terms/title> "A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy." <http://purl.org/np/RAuCkR_W8_jbTlpDJ-_lzcVfyLZdHhq5l6SpN2iMEE3as#provenance> .
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