Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_provenance.
- NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_provenance.
- NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_assertion evidence source_evidence_literature NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_provenance.
- NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_assertion SIO_000772 20622878 NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_provenance.
- NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_assertion wasDerivedFrom gad-20150221 NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_provenance.
- NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_assertion wasGeneratedBy ECO_0000203 NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP181068.RAcvZPSY4ReTzxgG_LeZubld5AZB0wf8PJZCkCEhuXgDI130_provenance.