Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_provenance.
- NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_assertion description "[We identified that an SNP rs12210050 at 6p25 near the EXOC2 gene was associated with an increased risk of BCC [rs12210050[T]: combined OR (95% CI), 1.24 (1.17-1.31); P= 9.9 � 10(-10)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_provenance.
- NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_assertion evidence source_evidence_literature NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_provenance.
- NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_assertion SIO_000772 21700618 NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_provenance.
- NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_assertion wasDerivedFrom befree-20150227 NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_provenance.
- NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_assertion wasGeneratedBy ECO_0000203 NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP920893.RA1k_xCe5nIaAMXsDi6ZJP98lzD1TaQggcwCyjR8x-8VI130_provenance.