Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_provenance.
- NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_assertion description "[Protein phosphorylation corrects the folding defect of the neuroblastoma (S120G) mutant of human nucleoside diphosphate kinase A/Nm23-H1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_provenance.
- NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_assertion evidence source_evidence_literature NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_provenance.
- NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_assertion SIO_000772 17155928 NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_provenance.
- NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_assertion wasDerivedFrom befree-2016 NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_provenance.
- NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_assertion wasGeneratedBy ECO_0000203 NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_provenance.
- befree-2016 importedOn "2016-02-19" NP583277.RAPNwbvw-XvWt4x1wXLfuQsoBMFGwGcdI3sGSNSRpcPqk130_provenance.