Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_provenance.
- befree-2016 importedOn "2016-02-19" NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_provenance.
- NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_assertion wasGeneratedBy ECO_0000203 NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_provenance.
- NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_assertion wasDerivedFrom befree-2016 NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_provenance.
- NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_assertion SIO_000772 21196064 NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_provenance.
- NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_assertion evidence source_evidence_literature NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_provenance.
- NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_assertion description "[Cognitively normal control subjects (n = 170) and AD patients (n = 92) were genotyped for 19 putative regulatory tagging SNPs within 9 genes (APP, ADAM10, BACE1, BACE2, PSEN1, PSEN2, PEN2, NCSTN and APH1B) involved in the APP processing pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862430.RAg4EkfWNfdPhtnK2r37Zs3L6TSUYbxzQCsjkQttw-cgA130_provenance.