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<http://identifiers.org/ensembl/ENSG00000101871> <http://www.w3.org/2000/01/rdf-schema#label> "MID1" <http://purl.org/np/RAf8ST-vaTiXwMcMVfxqClAip2lLaun8DJdW9vAGSgN_o#assertion> .
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<http://identifiers.org/pubmed/9354791> <http://purl.org/dc/terms/title> "Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22" <http://purl.org/np/RAf8ST-vaTiXwMcMVfxqClAip2lLaun8DJdW9vAGSgN_o#provenance> .
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<http://purl.org/np/RAf8ST-vaTiXwMcMVfxqClAip2lLaun8DJdW9vAGSgN_o> <http://purl.org/pav/authoredBy> <http://orcid.org/0000-0002-7770-620X> <http://purl.org/np/RAf8ST-vaTiXwMcMVfxqClAip2lLaun8DJdW9vAGSgN_o#publicationInfo> .
<http://purl.org/np/RAf8ST-vaTiXwMcMVfxqClAip2lLaun8DJdW9vAGSgN_o> <http://purl.org/pav/createdBy> <http://orcid.org/0000-0001-7542-0286> <http://purl.org/np/RAf8ST-vaTiXwMcMVfxqClAip2lLaun8DJdW9vAGSgN_o#publicationInfo> .
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