http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4#head http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4#assertion http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4#provenance http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4#assertion http://rdf.disgenet.org/resource/gda/DGNa6a45d2e6da87570d4da2945de0c963f http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/2934 http://rdf.disgenet.org/resource/gda/DGNa6a45d2e6da87570d4da2945de0c963f http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0162534 http://rdf.disgenet.org/resource/gda/DGNa6a45d2e6da87570d4da2945de0c963f http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001121 http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4#provenance http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4#assertion http://purl.org/dc/terms/description [CAA occurs in several familial conditions, including hereditary cerebral hemorrhage with amyloidosis of Icelandic type caused by deposition of mutant cystatin C, hereditary cerebral hemorrhage with amyloidosis Dutch type and familial AD with deposition of either A beta variants or wild-type A beta, the transthyretin-related meningo-vascular amyloidoses, gelsolin as well as familial prion disease-related CAAs and the recently described BRI2 gene-related CAAs in familial British dementia and familial Danish dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4#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/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/12146803 http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4#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/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://purl.org/dc/terms/created 2017-10-17T13:13:07+02:00 http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP461257.RAVV8EOUMdg5EJ_N7uugas7092uOLoQitXMtFH4e8wQz4 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