http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o#head http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o#assertion http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o#provenance http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o#assertion http://rdf.disgenet.org/resource/gda/DGN182ed4e04636831199d8fe3b08aaeb94 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/10452 http://rdf.disgenet.org/resource/gda/DGN182ed4e04636831199d8fe3b08aaeb94 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0002395 http://rdf.disgenet.org/resource/gda/DGN182ed4e04636831199d8fe3b08aaeb94 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o#provenance http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o#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/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o#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/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/25948718 http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o#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/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://purl.org/dc/terms/created 2017-10-17T13:17:56+02:00 http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1216488.RAzdQ8qmLtrd6cAeezlEeWZEqpMSQ0k92cR_SWzqW-x4o 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