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<http://identifiers.org/ensembl/ENSG00000132031> <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/RA2tisTmpO364iF0gxn_GXR2JBb1mH_NMFhOSLVULkwqI#assertion> .
<http://identifiers.org/ensembl/ENSG00000132031> <http://www.w3.org/2000/01/rdf-schema#label> "MATN3" <http://purl.org/np/RA2tisTmpO364iF0gxn_GXR2JBb1mH_NMFhOSLVULkwqI#assertion> .
<http://purl.org/np/RA2tisTmpO364iF0gxn_GXR2JBb1mH_NMFhOSLVULkwqI#association> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ensembl/ENSG00000132031> <http://purl.org/np/RA2tisTmpO364iF0gxn_GXR2JBb1mH_NMFhOSLVULkwqI#assertion> .
<http://purl.org/np/RA2tisTmpO364iF0gxn_GXR2JBb1mH_NMFhOSLVULkwqI#association> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/omim/607078> <http://purl.org/np/RA2tisTmpO364iF0gxn_GXR2JBb1mH_NMFhOSLVULkwqI#assertion> .
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<http://identifiers.org/pubmed/11479597> <http://purl.org/dc/terms/title> "Mutations in the region encoding the von Willebrand factor A domain of matrilin-3 are associated with multiple epiphyseal dysplasia." <http://purl.org/np/RA2tisTmpO364iF0gxn_GXR2JBb1mH_NMFhOSLVULkwqI#provenance> .
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