http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM#head http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM#assertion http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM#provenance http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM#assertion http://rdf.disgenet.org/resource/gda/DGN317636e13dc19155c514af711e231087 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/348 http://rdf.disgenet.org/resource/gda/DGN317636e13dc19155c514af711e231087 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0497327 http://rdf.disgenet.org/resource/gda/DGN317636e13dc19155c514af711e231087 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM#provenance http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM#assertion http://purl.org/dc/terms/description [The multifactorial genetic dysfunction in dementia includes mutational loci (APP, PS1, PS2, TAU) and diverse susceptibility loci (APOE, alpha2M, alphaACT, LRP1, IL1 alpha, TNF, ACE, BACE, BCHE, CST3, MTHFR, GSK3 beta, NOS3 and many other genes) distributed across the human genome, probably converging in a common pathogenic mechanism that leads to premature neuronal death, in which mitochondrial DNA mutations may contribute to increased genetic variability and heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/16470248 http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://purl.org/dc/terms/created 2017-10-17T13:10:36+02:00 http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP63977.RAnQsnetiAO-xXo_ILNecEtHuxcLunUO15DH_V7Ihz7bM http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0