@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP200942.RAmg-Bx2l6XiqPmrQO2b39OGYEj3pK1ueOfssJ3GT7oPo
> .
@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:NP200942.RAmg-Bx2l6XiqPmrQO2b39OGYEj3pK1ueOfssJ3GT7oPo130_head
{
this:
np:hasAssertion
dgn-np:NP200942.RAmg-Bx2l6XiqPmrQO2b39OGYEj3pK1ueOfssJ3GT7oPo130_assertion
;
np:hasProvenance
dgn-np:NP200942.RAmg-Bx2l6XiqPmrQO2b39OGYEj3pK1ueOfssJ3GT7oPo130_provenance
;
np:hasPublicationInfo
dgn-np:NP200942.RAmg-Bx2l6XiqPmrQO2b39OGYEj3pK1ueOfssJ3GT7oPo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP200942.RAmg-Bx2l6XiqPmrQO2b39OGYEj3pK1ueOfssJ3GT7oPo130_assertion
a
np:Assertion
.
dgn-np:NP200942.RAmg-Bx2l6XiqPmrQO2b39OGYEj3pK1ueOfssJ3GT7oPo130_provenance
a
np:Provenance
.
dgn-np:NP200942.RAmg-Bx2l6XiqPmrQO2b39OGYEj3pK1ueOfssJ3GT7oPo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP200942.RAmg-Bx2l6XiqPmrQO2b39OGYEj3pK1ueOfssJ3GT7oPo130_assertion
{
miriam-gene:1917
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNef63cbd18518b31131ea9f9883a75367
sio:SIO_000628
miriam-gene:1917
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP200942.RAmg-Bx2l6XiqPmrQO2b39OGYEj3pK1ueOfssJ3GT7oPo130_provenance
{
dgn-np:NP200942.RAmg-Bx2l6XiqPmrQO2b39OGYEj3pK1ueOfssJ3GT7oPo130_assertion
dcterms:description
"[The motor abnormalities of Parkinson's disease (PD) are caused by alterations in basal ganglia network activity, including disinhibition of the subthalamic nucleus (STN), and excessive activity of the major output nuclei.]. 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:12376704
;
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:NP200942.RAmg-Bx2l6XiqPmrQO2b39OGYEj3pK1ueOfssJ3GT7oPo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:51+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" .
}