@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_head
{
this:
np:hasAssertion
dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_assertion
;
np:hasProvenance
dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_provenance
;
np:hasPublicationInfo
dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_assertion
a
np:Assertion
.
dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_provenance
a
np:Provenance
.
dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0043528
a
ncit:C7057
.
dgn-gda:DGN41b631305ce3f549ff38b12811b75346
sio:SIO_000628
miriam-gene:5621
,
lld:C0043528
;
a
sio:SIO_001121
.
}
dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_provenance
{
dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_assertion
dcterms:description
"[The cause of sporadic Creutzfeldt-Jakob disease (CJD) is unknown, hereditary cases are associated with mutations of the prion protein gene (PRNP) and acquired forms are caused by the transmission of infection from human to human or, as a zoonosis, from cattle to human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:14522863
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:08+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetv3.0rdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}