Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_provenance.
- NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_assertion description "[Besides, there is no report about the association between NBS1 3'UTR variant rs2735383 and ALL risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_provenance.
- NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_assertion evidence source_evidence_literature NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_provenance.
- NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_assertion SIO_000772 21166880 NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_provenance.
- NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_assertion wasDerivedFrom befree-20140225 NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_provenance.
- NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_assertion wasGeneratedBy ECO_0000203 NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP874425.RAjOsiu20BSsJ7UWtPiO9a5jLrt8WSN5SUekH6hgTLjkM130_provenance.