Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_provenance.
- NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_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." NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_provenance.
- NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_assertion evidence source_evidence_literature NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_provenance.
- NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_assertion SIO_000772 21700618 NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_provenance.
- NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_assertion wasDerivedFrom befree-20140225 NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_provenance.
- NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_assertion wasGeneratedBy ECO_0000203 NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP897143.RA9z6aEKQk-yM4oFdLwKmvSKGnQWgRkPDKqLXiZ37vfS8130_provenance.