Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_provenance.
- NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_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." NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_provenance.
- NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_assertion evidence source_evidence_literature NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_provenance.
- NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_assertion SIO_000772 17903303 NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_provenance.
- NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_assertion wasDerivedFrom gad-20150221 NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_provenance.
- NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_assertion wasGeneratedBy ECO_0000203 NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP157635.RAanZVb4yESol_hUHLn1VLog4hDkESr-njL3SLBErQeOg130_provenance.