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- NP334068.RAxz-aSNXCWUMairIF3FntBjIv1BE4OrvgcMkMvBN2pdk130_assertion type Assertion NP334068.RAxz-aSNXCWUMairIF3FntBjIv1BE4OrvgcMkMvBN2pdk130_head.
- NP334068.RAxz-aSNXCWUMairIF3FntBjIv1BE4OrvgcMkMvBN2pdk130_assertion description "[Clinical experience has suggested that patients with the contiguous gene syndrome, complex glycerol kinase deficiency (cGKD), will have mental retardation (MR) if they have deletions extending from the GK gene into the DMD gene and/or involving a significant extension telomeric from DAX1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP334068.RAxz-aSNXCWUMairIF3FntBjIv1BE4OrvgcMkMvBN2pdk130_provenance.
- NP334068.RAxz-aSNXCWUMairIF3FntBjIv1BE4OrvgcMkMvBN2pdk130_assertion evidence source_evidence_literature NP334068.RAxz-aSNXCWUMairIF3FntBjIv1BE4OrvgcMkMvBN2pdk130_provenance.
- NP334068.RAxz-aSNXCWUMairIF3FntBjIv1BE4OrvgcMkMvBN2pdk130_assertion SIO_000772 15300857 NP334068.RAxz-aSNXCWUMairIF3FntBjIv1BE4OrvgcMkMvBN2pdk130_provenance.
- NP334068.RAxz-aSNXCWUMairIF3FntBjIv1BE4OrvgcMkMvBN2pdk130_assertion wasDerivedFrom befree-20140225 NP334068.RAxz-aSNXCWUMairIF3FntBjIv1BE4OrvgcMkMvBN2pdk130_provenance.
- NP334068.RAxz-aSNXCWUMairIF3FntBjIv1BE4OrvgcMkMvBN2pdk130_assertion wasGeneratedBy ECO_0000203 NP334068.RAxz-aSNXCWUMairIF3FntBjIv1BE4OrvgcMkMvBN2pdk130_provenance.