Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_provenance.
- NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_assertion description "[The association with an SNP located 3' near CRY1 gene in MDD remained statistically significant after permutation correction at experiment level (p=0.007).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_provenance.
- NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_assertion evidence source_evidence_literature NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_provenance.
- NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_assertion SIO_000772 20072116 NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_provenance.
- NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_assertion wasDerivedFrom befree-2016 NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_provenance.
- NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_assertion wasGeneratedBy ECO_0000203 NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_provenance.
- befree-2016 importedOn "2016-02-19" NP786906.RAfLbEbRJalrxPsBeViDfVLVjOX5TYXUnhgYtjJEVsEWk130_provenance.