http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA#head http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA#assertion http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA#provenance http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA#assertion http://rdf.disgenet.org/resource/gda/DGNce93c37926c6b03f0092a044a5797e79 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/5621 http://rdf.disgenet.org/resource/gda/DGNce93c37926c6b03f0092a044a5797e79 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0338656 http://rdf.disgenet.org/resource/gda/DGNce93c37926c6b03f0092a044a5797e79 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001121 http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA#provenance http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA#assertion http://purl.org/dc/terms/description [Fatal familial insomnia (FFI) is an inherited prion disease characterized by progressive insomnia and dysautonomia with only modest cognitive impairment early in the disease, associated with atrophy and gliosis in the medial thalamus, but without spongiform change.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA#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/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/9270595 http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA#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/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://purl.org/dc/terms/created 2017-10-17T13:15:40+02:00 http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP862133.RA7r8pdHbaqTZHy3KTJ0VmV8YVCUwd-pu2GyzbFTw6IgA 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