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