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<http://identifiers.org/ensembl/ENSG00000187098> <http://www.w3.org/2000/01/rdf-schema#label> "MITF" <http://purl.org/np/RAMrqzc9abF31CTN0B404_7RSeLYKBo-BO0ufcjjlBq8g#assertion> .
<http://purl.org/np/RAMrqzc9abF31CTN0B404_7RSeLYKBo-BO0ufcjjlBq8g#association> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ensembl/ENSG00000187098> <http://purl.org/np/RAMrqzc9abF31CTN0B404_7RSeLYKBo-BO0ufcjjlBq8g#assertion> .
<http://purl.org/np/RAMrqzc9abF31CTN0B404_7RSeLYKBo-BO0ufcjjlBq8g#association> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/omim/193510> <http://purl.org/np/RAMrqzc9abF31CTN0B404_7RSeLYKBo-BO0ufcjjlBq8g#assertion> .
<http://purl.org/np/RAMrqzc9abF31CTN0B404_7RSeLYKBo-BO0ufcjjlBq8g#association> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_000983> <http://purl.org/np/RAMrqzc9abF31CTN0B404_7RSeLYKBo-BO0ufcjjlBq8g#assertion> .
<http://identifiers.org/pubmed/7874167> <http://purl.org/dc/terms/title> "Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene." <http://purl.org/np/RAMrqzc9abF31CTN0B404_7RSeLYKBo-BO0ufcjjlBq8g#provenance> .
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