@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk
> .
@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:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_head
{
this:
np:hasAssertion
dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_assertion
;
np:hasProvenance
dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_provenance
;
np:hasPublicationInfo
dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_assertion
a
np:Assertion
.
dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_provenance
a
np:Provenance
.
dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGNf14b4a5b85d0b9c6cd39407fe493962d
sio:SIO_000628
miriam-gene:1813
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_provenance
{
dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_assertion
dcterms:description
"[XDP has certain similarities to Huntington disease not only in pathological and clinical findings, but also the molecular mechanism, which disturbs expression of genes essential for striatal neurons, such as DRD2.]. 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:16366515
;
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:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:55+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" .
}