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- source_evidence_literature type ECO_0000212 NP919325.RAKVXxYhVY1x2oBA7pXNsZlx0QcAuDBWxMNd4_Lx8T9UE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919325.RAKVXxYhVY1x2oBA7pXNsZlx0QcAuDBWxMNd4_Lx8T9UE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919325.RAKVXxYhVY1x2oBA7pXNsZlx0QcAuDBWxMNd4_Lx8T9UE130_provenance.
- NP919325.RAKVXxYhVY1x2oBA7pXNsZlx0QcAuDBWxMNd4_Lx8T9UE130_assertion description "[In this study, we tested 27 genes (ACE, BDNF, CH25H, CHRNB2, CST3, CTSD, DAPK1, GALP, hCG2039140, IL1B, LMNA, LOC439999, LOC651924, MAPT, MTHFR, MYH13, PCK1, PGBD1, PRNP, PSEN1, SORCS1, SORL1, TF, TFAM, TNK1, GWA_14q32.13, and GWA_7p15.2), all showing significant association with AD risk in the AlzGene meta-analyses, in a large collection of family-based samples comprised of 4,180 subjects from over 1,300 pedigrees.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919325.RAKVXxYhVY1x2oBA7pXNsZlx0QcAuDBWxMNd4_Lx8T9UE130_provenance.
- NP919325.RAKVXxYhVY1x2oBA7pXNsZlx0QcAuDBWxMNd4_Lx8T9UE130_assertion evidence source_evidence_literature NP919325.RAKVXxYhVY1x2oBA7pXNsZlx0QcAuDBWxMNd4_Lx8T9UE130_provenance.
- NP919325.RAKVXxYhVY1x2oBA7pXNsZlx0QcAuDBWxMNd4_Lx8T9UE130_assertion SIO_000772 18830724 NP919325.RAKVXxYhVY1x2oBA7pXNsZlx0QcAuDBWxMNd4_Lx8T9UE130_provenance.
- NP919325.RAKVXxYhVY1x2oBA7pXNsZlx0QcAuDBWxMNd4_Lx8T9UE130_assertion wasDerivedFrom befree-20140225 NP919325.RAKVXxYhVY1x2oBA7pXNsZlx0QcAuDBWxMNd4_Lx8T9UE130_provenance.
- NP919325.RAKVXxYhVY1x2oBA7pXNsZlx0QcAuDBWxMNd4_Lx8T9UE130_assertion wasGeneratedBy ECO_0000203 NP919325.RAKVXxYhVY1x2oBA7pXNsZlx0QcAuDBWxMNd4_Lx8T9UE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP919325.RAKVXxYhVY1x2oBA7pXNsZlx0QcAuDBWxMNd4_Lx8T9UE130_provenance.