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- source_evidence_literature type ECO_0000212 NP212055.RATAldz_mZnZTQutyjgnQ6XAynIHMswMkMWJSxQ-va1Ug130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212055.RATAldz_mZnZTQutyjgnQ6XAynIHMswMkMWJSxQ-va1Ug130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212055.RATAldz_mZnZTQutyjgnQ6XAynIHMswMkMWJSxQ-va1Ug130_provenance.
- NP212055.RATAldz_mZnZTQutyjgnQ6XAynIHMswMkMWJSxQ-va1Ug130_assertion wasGeneratedBy ECO_0000203 NP212055.RATAldz_mZnZTQutyjgnQ6XAynIHMswMkMWJSxQ-va1Ug130_provenance.
- NP212055.RATAldz_mZnZTQutyjgnQ6XAynIHMswMkMWJSxQ-va1Ug130_assertion wasDerivedFrom befree-20140225 NP212055.RATAldz_mZnZTQutyjgnQ6XAynIHMswMkMWJSxQ-va1Ug130_provenance.
- NP212055.RATAldz_mZnZTQutyjgnQ6XAynIHMswMkMWJSxQ-va1Ug130_assertion SIO_000772 16423463 NP212055.RATAldz_mZnZTQutyjgnQ6XAynIHMswMkMWJSxQ-va1Ug130_provenance.
- NP212055.RATAldz_mZnZTQutyjgnQ6XAynIHMswMkMWJSxQ-va1Ug130_assertion evidence source_evidence_literature NP212055.RATAldz_mZnZTQutyjgnQ6XAynIHMswMkMWJSxQ-va1Ug130_provenance.
- NP212055.RATAldz_mZnZTQutyjgnQ6XAynIHMswMkMWJSxQ-va1Ug130_assertion description "[Furthermore, we found an intronic +17G>C polymorphism in PEN2 which, in homozygous form, was greater in early onset Alzheimer's disease (EOAD) compared to controls, and one haplotype in the NCSTN gene which was linked to EOAD and familial AD (FAD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212055.RATAldz_mZnZTQutyjgnQ6XAynIHMswMkMWJSxQ-va1Ug130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212055.RATAldz_mZnZTQutyjgnQ6XAynIHMswMkMWJSxQ-va1Ug130_provenance.