Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP455175.RAtIqJBpp-piBAbZhstis622mfCsZkTt2R6YavzmgrC1Y130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP455175.RAtIqJBpp-piBAbZhstis622mfCsZkTt2R6YavzmgrC1Y130_assertion type Assertion NP455175.RAtIqJBpp-piBAbZhstis622mfCsZkTt2R6YavzmgrC1Y130_head.
- NP455175.RAtIqJBpp-piBAbZhstis622mfCsZkTt2R6YavzmgrC1Y130_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." NP455175.RAtIqJBpp-piBAbZhstis622mfCsZkTt2R6YavzmgrC1Y130_provenance.
- NP455175.RAtIqJBpp-piBAbZhstis622mfCsZkTt2R6YavzmgrC1Y130_assertion evidence source_evidence_literature NP455175.RAtIqJBpp-piBAbZhstis622mfCsZkTt2R6YavzmgrC1Y130_provenance.
- NP455175.RAtIqJBpp-piBAbZhstis622mfCsZkTt2R6YavzmgrC1Y130_assertion SIO_000772 15300857 NP455175.RAtIqJBpp-piBAbZhstis622mfCsZkTt2R6YavzmgrC1Y130_provenance.
- NP455175.RAtIqJBpp-piBAbZhstis622mfCsZkTt2R6YavzmgrC1Y130_assertion wasDerivedFrom befree-2016 NP455175.RAtIqJBpp-piBAbZhstis622mfCsZkTt2R6YavzmgrC1Y130_provenance.
- NP455175.RAtIqJBpp-piBAbZhstis622mfCsZkTt2R6YavzmgrC1Y130_assertion wasGeneratedBy ECO_0000203 NP455175.RAtIqJBpp-piBAbZhstis622mfCsZkTt2R6YavzmgrC1Y130_provenance.