Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_provenance.
- NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identi]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_provenance.
- NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_assertion evidence source_evidence_literature NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_provenance.
- NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_assertion SIO_000772 17903303 NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_provenance.
- NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_assertion wasDerivedFrom gad-20150221 NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_provenance.
- NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_assertion wasGeneratedBy ECO_0000203 NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_provenance.
- gad-20150221 importedOn "2015-02-21" NP157671.RAojEdnR102pIROWDLwE8kXAJ5eY9saM8WdU2c1H8NY28130_provenance.