http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0#head http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0#assertion http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0#provenance http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0#assertion http://rdf.disgenet.org/resource/gda/DGN41689b1fda6ca75f17600f24b843015f http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/351 http://rdf.disgenet.org/resource/gda/DGN41689b1fda6ca75f17600f24b843015f http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0276496 http://rdf.disgenet.org/resource/gda/DGN41689b1fda6ca75f17600f24b843015f http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0#provenance http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0#assertion http://purl.org/dc/terms/description [The presence or absence of endocytic abnormalities distinguish subtypes of familial Alzheimer's disease linked to APP mutations from presenilin mutations, supporting the notion that different cellular pathways are involved in the altered processing of APP leading to increased beta-amyloid generation in certain of these different Alzheimer's disease subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0#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/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/11706973 http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0#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/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://purl.org/dc/terms/created 2017-10-17T13:10:38+02:00 http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP70203.RA2LDc7VRb8RaWMTDNJhubPl3_vI6vdyESJdFHxuiXJo0 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