http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE#head
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE#assertion
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE#provenance
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE#assertion
http://rdf.disgenet.org/resource/gda/DGN13686c35b4a0dce3fe0470c2d5095db7
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/351
http://rdf.disgenet.org/resource/gda/DGN13686c35b4a0dce3fe0470c2d5095db7
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0002395
http://rdf.disgenet.org/resource/gda/DGN13686c35b4a0dce3fe0470c2d5095db7
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE#provenance
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE#assertion
http://purl.org/dc/terms/description
[Some cases of AD, particularly those of early onset, are familial and inherited as autosomal dominant disorders linked to the presence of mutant genes that encode the amyloid precursor protein (APP) or the presenilins (PS1 or PS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE#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/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/9530504
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE#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/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://purl.org/dc/terms/created
2017-10-17T13:10:39+02:00
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP71899.RAnks0U-fgX5se062nQ4xUgGFeAhosYEZWkVzAS-Hn3SE
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