Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_provenance.
- NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_assertion description "[We hypothesized that functional polymorphisms in GSTT1 (gene deletion) and CYP1A1 (m1, m2, and m3) might be associated with SIDS risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_provenance.
- NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_assertion evidence source_evidence_literature NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_provenance.
- NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_assertion SIO_000772 16763966 NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_provenance.
- NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_assertion wasDerivedFrom befree-20140225 NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_provenance.
- NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_assertion wasGeneratedBy ECO_0000203 NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP532506.RA4-QMFPdIzlQIk3ExP9ZNyoqg9iV6TCcuS-OY-jP3QKA130_provenance.