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<http://purl.org/np/RA9uoEoaSuAK646Uu5YwrWOWummnT2NY-TSv4EoHhh12A> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#Nanopublication> <http://purl.org/np/RA9uoEoaSuAK646Uu5YwrWOWummnT2NY-TSv4EoHhh12A#head> .
<http://identifiers.org/ensembl/ENSG00000173614> <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/RA9uoEoaSuAK646Uu5YwrWOWummnT2NY-TSv4EoHhh12A#assertion> .
<http://identifiers.org/ensembl/ENSG00000173614> <http://www.w3.org/2000/01/rdf-schema#label> "NMNAT1" <http://purl.org/np/RA9uoEoaSuAK646Uu5YwrWOWummnT2NY-TSv4EoHhh12A#assertion> .
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<http://purl.org/np/RA9uoEoaSuAK646Uu5YwrWOWummnT2NY-TSv4EoHhh12A#association> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_000983> <http://purl.org/np/RA9uoEoaSuAK646Uu5YwrWOWummnT2NY-TSv4EoHhh12A#assertion> .
<http://identifiers.org/pubmed/22842230> <http://purl.org/dc/terms/title> "Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration" <http://purl.org/np/RA9uoEoaSuAK646Uu5YwrWOWummnT2NY-TSv4EoHhh12A#provenance> .
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<http://purl.org/np/RA9uoEoaSuAK646Uu5YwrWOWummnT2NY-TSv4EoHhh12A> <http://purl.org/dc/terms/created> "2018-04-05T10:17:11.353+02:00"^^<http://www.w3.org/2001/XMLSchema#dateTime> <http://purl.org/np/RA9uoEoaSuAK646Uu5YwrWOWummnT2NY-TSv4EoHhh12A#publicationInfo> .
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