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<http://identifiers.org/ensembl/ENSG00000143183> <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/RADL1-BWGCSbbfJLpBT_JEqzgRYLwdZrTM7X3AQMVxML8#assertion> .
<http://identifiers.org/ensembl/ENSG00000143183> <http://www.w3.org/2000/01/rdf-schema#label> "TMCO1" <http://purl.org/np/RADL1-BWGCSbbfJLpBT_JEqzgRYLwdZrTM7X3AQMVxML8#assertion> .
<http://purl.org/np/RADL1-BWGCSbbfJLpBT_JEqzgRYLwdZrTM7X3AQMVxML8#association> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ensembl/ENSG00000143183> <http://purl.org/np/RADL1-BWGCSbbfJLpBT_JEqzgRYLwdZrTM7X3AQMVxML8#assertion> .
<http://purl.org/np/RADL1-BWGCSbbfJLpBT_JEqzgRYLwdZrTM7X3AQMVxML8#association> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/omim/213980> <http://purl.org/np/RADL1-BWGCSbbfJLpBT_JEqzgRYLwdZrTM7X3AQMVxML8#assertion> .
<http://purl.org/np/RADL1-BWGCSbbfJLpBT_JEqzgRYLwdZrTM7X3AQMVxML8#association> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_000983> <http://purl.org/np/RADL1-BWGCSbbfJLpBT_JEqzgRYLwdZrTM7X3AQMVxML8#assertion> .
<http://identifiers.org/pubmed/20018682> <http://purl.org/dc/terms/title> "Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation." <http://purl.org/np/RADL1-BWGCSbbfJLpBT_JEqzgRYLwdZrTM7X3AQMVxML8#provenance> .
<http://purl.org/np/RADL1-BWGCSbbfJLpBT_JEqzgRYLwdZrTM7X3AQMVxML8#assertion> <http://semanticscience.org/resource/SIO_000253> <http://identifiers.org/pubmed/20018682> <http://purl.org/np/RADL1-BWGCSbbfJLpBT_JEqzgRYLwdZrTM7X3AQMVxML8#provenance> .
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<http://purl.org/np/RADL1-BWGCSbbfJLpBT_JEqzgRYLwdZrTM7X3AQMVxML8> <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/RADL1-BWGCSbbfJLpBT_JEqzgRYLwdZrTM7X3AQMVxML8#publicationInfo> .
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