Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_provenance.
- NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_assertion description "[Combination of NAT2 fast acetylator and GSTM1 null genotype posed a significantly increased risk of MM in the Italian, but not in the Finnish study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_provenance.
- NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_assertion evidence source_evidence_literature NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_provenance.
- NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_assertion SIO_000772 16697254 NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_provenance.
- NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_assertion wasDerivedFrom befree-2016 NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_provenance.
- NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_assertion wasGeneratedBy ECO_0000203 NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_provenance.
- befree-2016 importedOn "2016-02-19" NP549485.RA52ilSDygKin7mBvBjYr9b13QdDez7cMV3OjYcLOX7Rg130_provenance.