@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1340911.RAHda9zIKZq6HyM99uk9syDAPD2VSxBjLB7vCnUdnM4f0
> .
@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/v4.0.0/void/
> .
dgn-np:NP1340911.RAHda9zIKZq6HyM99uk9syDAPD2VSxBjLB7vCnUdnM4f0130_head
{
this:
np:hasAssertion
dgn-np:NP1340911.RAHda9zIKZq6HyM99uk9syDAPD2VSxBjLB7vCnUdnM4f0130_assertion
;
np:hasProvenance
dgn-np:NP1340911.RAHda9zIKZq6HyM99uk9syDAPD2VSxBjLB7vCnUdnM4f0130_provenance
;
np:hasPublicationInfo
dgn-np:NP1340911.RAHda9zIKZq6HyM99uk9syDAPD2VSxBjLB7vCnUdnM4f0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1340911.RAHda9zIKZq6HyM99uk9syDAPD2VSxBjLB7vCnUdnM4f0130_assertion
a
np:Assertion
.
dgn-np:NP1340911.RAHda9zIKZq6HyM99uk9syDAPD2VSxBjLB7vCnUdnM4f0130_provenance
a
np:Provenance
.
dgn-np:NP1340911.RAHda9zIKZq6HyM99uk9syDAPD2VSxBjLB7vCnUdnM4f0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1340911.RAHda9zIKZq6HyM99uk9syDAPD2VSxBjLB7vCnUdnM4f0130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0162534
a
ncit:C7057
.
dgn-gda:DGN69d42ba7673e52e593bfb0c733da2b4d
sio:SIO_000628
miriam-gene:5621
,
lld:C0162534
;
a
sio:SIO_001121
.
}
dgn-np:NP1340911.RAHda9zIKZq6HyM99uk9syDAPD2VSxBjLB7vCnUdnM4f0130_provenance
{
dgn-np:NP1340911.RAHda9zIKZq6HyM99uk9syDAPD2VSxBjLB7vCnUdnM4f0130_assertion
dcterms:description
"[The identification of pathogenic mutations in the PrP gene has enabled the identification of cases of inherited prion disease that would not have been recognised using existing clinical and pathological diagnostic criteria.]. 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:8401789
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1340911.RAHda9zIKZq6HyM99uk9syDAPD2VSxBjLB7vCnUdnM4f0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:54+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}