Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_provenance.
- NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_assertion description "[In a case (n = 928)-control (n = 843) study of breast cancer in AA and EA women, we measured serum 25OHD levels in controls and tested associations between risk and tag single nucleotide polymorphisms (SNPs) in VDR, CYP24A1 and CYP27B1, particularly by ER status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_provenance.
- NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_assertion evidence source_evidence_literature NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_provenance.
- NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_assertion SIO_000772 22480149 NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_provenance.
- NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_assertion wasDerivedFrom befree-2016 NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_provenance.
- NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_assertion wasGeneratedBy ECO_0000203 NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_provenance.
- befree-2016 importedOn "2016-02-19" NP972901.RASLWcCF-HaGmuprkdbW2rgn_a5G3F1FDVn-ly6MhzXcc130_provenance.