Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_provenance.
- NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_assertion description "[Although these findings may represent a random chance event, in view of previous reports of linkage and association of this gene region to AITD, this may be an example of a rare causal variant of a complex disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_provenance.
- NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_assertion evidence source_evidence_literature NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_provenance.
- NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_assertion SIO_000772 14557492 NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_provenance.
- NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_assertion wasDerivedFrom gad-20150221 NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_provenance.
- NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_assertion wasGeneratedBy ECO_0000203 NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP62941.RArqVoTk6iAKUTRmmoBM4tel8UcJPCXKKZiKrOEaaQRGQ130_provenance.