http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck#head http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck#assertion http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck#provenance http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck#assertion http://rdf.disgenet.org/resource/gda/DGN0d1d0a2541bbc26f0232479562160f48 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/54209 http://rdf.disgenet.org/resource/gda/DGN0d1d0a2541bbc26f0232479562160f48 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0002395 http://rdf.disgenet.org/resource/gda/DGN0d1d0a2541bbc26f0232479562160f48 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck#provenance http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck#assertion http://purl.org/dc/terms/description [Our findings, also supported by the ?-amyloid plasma assay, confirm (1) the pathogenic role of the APP A713T mutation, (2) the specific phenotype (AD with cerebrovascular lesions) associated with this mutation, and (3) the large span of age at onset, not influenced by APOE, TOMM40, and TREM2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck#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/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/25948718 http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck#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/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://purl.org/dc/terms/created 2017-10-17T13:18:34+02:00 http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1319264.RAJgxPhivx3O9mJ6nbse2YFDGfCV3mc1BPS1e_SBZYCck 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