Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_provenance.
- NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_assertion description "[Two polymorphisms were associated with T2DM susceptibility: in particular, the G allele of rs895819 in hsa-mir-27a has shown a significantly protective effect (OR = 0.58 and P = 0.008), while the G allele of rs531564 in hsa-mir-124a appears to be a risk allele (OR = 2.15, P = 0.008).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_provenance.
- NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_assertion evidence source_evidence_literature NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_provenance.
- NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_assertion SIO_000772 23532299 NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_provenance.
- NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_assertion wasDerivedFrom befree-20150227 NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_provenance.
- NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_assertion wasGeneratedBy ECO_0000203 NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP999417.RA1PCTQGRv7JMuHmJK-UKa1QlEb2_6BtuCnaKSuRN-PaI130_provenance.