Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_provenance.
- NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_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." NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_provenance.
- NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_assertion evidence source_evidence_literature NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_provenance.
- NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_assertion SIO_000772 15300857 NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_provenance.
- NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_assertion wasDerivedFrom befree-20150227 NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_provenance.
- NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_assertion wasGeneratedBy ECO_0000203 NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP355318.RAKvM4OCe0uBuTa7kZrg9sGOu0DVRG416UaZ7XNMvWHy8130_provenance.