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- source_evidence_literature type ECO_0000212 NP760131.RA2vt01FI_3mZSG-xVW23V0d102w8QeDu2uaowPOOPPJs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760131.RA2vt01FI_3mZSG-xVW23V0d102w8QeDu2uaowPOOPPJs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760131.RA2vt01FI_3mZSG-xVW23V0d102w8QeDu2uaowPOOPPJs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP760131.RA2vt01FI_3mZSG-xVW23V0d102w8QeDu2uaowPOOPPJs130_provenance.
- NP760131.RA2vt01FI_3mZSG-xVW23V0d102w8QeDu2uaowPOOPPJs130_assertion wasGeneratedBy ECO_0000203 NP760131.RA2vt01FI_3mZSG-xVW23V0d102w8QeDu2uaowPOOPPJs130_provenance.
- NP760131.RA2vt01FI_3mZSG-xVW23V0d102w8QeDu2uaowPOOPPJs130_assertion wasDerivedFrom befree-20150227 NP760131.RA2vt01FI_3mZSG-xVW23V0d102w8QeDu2uaowPOOPPJs130_provenance.
- NP760131.RA2vt01FI_3mZSG-xVW23V0d102w8QeDu2uaowPOOPPJs130_assertion SIO_000772 24917535 NP760131.RA2vt01FI_3mZSG-xVW23V0d102w8QeDu2uaowPOOPPJs130_provenance.
- NP760131.RA2vt01FI_3mZSG-xVW23V0d102w8QeDu2uaowPOOPPJs130_assertion evidence source_evidence_literature NP760131.RA2vt01FI_3mZSG-xVW23V0d102w8QeDu2uaowPOOPPJs130_provenance.
- NP760131.RA2vt01FI_3mZSG-xVW23V0d102w8QeDu2uaowPOOPPJs130_assertion description "[As compared to patients with the TSC1 mutation, patients with the TSC2 mutation were younger (p = 0.02), more likely to have partial epilepsy (odds ratio (OR) 1.74, p = 0.0015), complex partial seizures (OR 2.03, p = 0.02), infantile spasms (IS) (OR 1.67, p = 0.01), subependymal giant-cell astrocytomas (SEGAs) (OR 1.64, p = 0.01), and intellectual disability (OR 2.90, p = 0.0002).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760131.RA2vt01FI_3mZSG-xVW23V0d102w8QeDu2uaowPOOPPJs130_provenance.