http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0#head http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0#assertion http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0#provenance http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0#assertion http://rdf.disgenet.org/resource/gda/DGN8353157c52374604ad2bc43aa99b1d47 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/5621 http://rdf.disgenet.org/resource/gda/DGN8353157c52374604ad2bc43aa99b1d47 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0017495 http://rdf.disgenet.org/resource/gda/DGN8353157c52374604ad2bc43aa99b1d47 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0#provenance http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0#assertion http://purl.org/dc/terms/description [Despite their experimental transmissibility, missense and insertional mutations in the prion protein gene are associated with both GSS and familial CJD, demonstrating that the human familial cases are autosomal dominant diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0#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/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/1677164 http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0#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/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://purl.org/dc/terms/created 2017-10-17T13:15:40+02:00 http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP860554.RAkKPtjOYpCjUyFjEoXKe3aW6PJmHjJRT7eZw3lcsGDv0 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