@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP160761.RA4Zt6spd4ac0Qa89jxzhgDI84dsrZHixVjrqoqYLhj8o
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP160761.RA4Zt6spd4ac0Qa89jxzhgDI84dsrZHixVjrqoqYLhj8o130_head
{
this:
np:hasAssertion
dgn-np:NP160761.RA4Zt6spd4ac0Qa89jxzhgDI84dsrZHixVjrqoqYLhj8o130_assertion
;
np:hasProvenance
dgn-np:NP160761.RA4Zt6spd4ac0Qa89jxzhgDI84dsrZHixVjrqoqYLhj8o130_provenance
;
np:hasPublicationInfo
dgn-np:NP160761.RA4Zt6spd4ac0Qa89jxzhgDI84dsrZHixVjrqoqYLhj8o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP160761.RA4Zt6spd4ac0Qa89jxzhgDI84dsrZHixVjrqoqYLhj8o130_assertion
a
np:Assertion
.
dgn-np:NP160761.RA4Zt6spd4ac0Qa89jxzhgDI84dsrZHixVjrqoqYLhj8o130_provenance
a
np:Provenance
.
dgn-np:NP160761.RA4Zt6spd4ac0Qa89jxzhgDI84dsrZHixVjrqoqYLhj8o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP160761.RA4Zt6spd4ac0Qa89jxzhgDI84dsrZHixVjrqoqYLhj8o130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0162534
a
ncit:C7057
.
dgn-gda:DGNe5406e085cc62f0c6a9ec59e11b193fb
sio:SIO_000628
miriam-gene:5621
,
lld:C0162534
;
a
sio:SIO_001121
.
}
dgn-np:NP160761.RA4Zt6spd4ac0Qa89jxzhgDI84dsrZHixVjrqoqYLhj8o130_provenance
{
dgn-np:NP160761.RA4Zt6spd4ac0Qa89jxzhgDI84dsrZHixVjrqoqYLhj8o130_assertion
dcterms:description
"[This observation raises the possibility that an unknown number of HD phenocopies are, in fact, familial prion diseases and argues that clinicians should consider screening for PrP mutations in individuals with HD-like diseases in which the characteristic HD (CAG)n repeat expansions are absent.]. 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:11593450
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP160761.RA4Zt6spd4ac0Qa89jxzhgDI84dsrZHixVjrqoqYLhj8o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}