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<http://purl.org/np/RAsTlWtVSjBEE_c1fFIhHmZaZk6iwdoh9shsPe2d5ENvs> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#Nanopublication> <http://purl.org/np/RAsTlWtVSjBEE_c1fFIhHmZaZk6iwdoh9shsPe2d5ENvs#head> .
<http://identifiers.org/ensembl/ENSG00000130226> <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/RAsTlWtVSjBEE_c1fFIhHmZaZk6iwdoh9shsPe2d5ENvs#assertion> .
<http://identifiers.org/ensembl/ENSG00000130226> <http://www.w3.org/2000/01/rdf-schema#label> "DPP6" <http://purl.org/np/RAsTlWtVSjBEE_c1fFIhHmZaZk6iwdoh9shsPe2d5ENvs#assertion> .
<http://purl.org/np/RAsTlWtVSjBEE_c1fFIhHmZaZk6iwdoh9shsPe2d5ENvs#association> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ensembl/ENSG00000130226> <http://purl.org/np/RAsTlWtVSjBEE_c1fFIhHmZaZk6iwdoh9shsPe2d5ENvs#assertion> .
<http://purl.org/np/RAsTlWtVSjBEE_c1fFIhHmZaZk6iwdoh9shsPe2d5ENvs#association> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/omim/616311> <http://purl.org/np/RAsTlWtVSjBEE_c1fFIhHmZaZk6iwdoh9shsPe2d5ENvs#assertion> .
<http://purl.org/np/RAsTlWtVSjBEE_c1fFIhHmZaZk6iwdoh9shsPe2d5ENvs#association> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_000983> <http://purl.org/np/RAsTlWtVSjBEE_c1fFIhHmZaZk6iwdoh9shsPe2d5ENvs#assertion> .
<http://identifiers.org/pubmed/23832105> <http://purl.org/dc/terms/title> "Loss-of-function variation in the DPP6 gene is associated with autosomal dominant microcephaly and mental retardation." <http://purl.org/np/RAsTlWtVSjBEE_c1fFIhHmZaZk6iwdoh9shsPe2d5ENvs#provenance> .
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<http://purl.org/np/RAsTlWtVSjBEE_c1fFIhHmZaZk6iwdoh9shsPe2d5ENvs> <http://purl.org/pav/authoredBy> <http://orcid.org/0000-0002-7770-620X> <http://purl.org/np/RAsTlWtVSjBEE_c1fFIhHmZaZk6iwdoh9shsPe2d5ENvs#publicationInfo> .
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