@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP624914.RA4kMjSZHkrM3GtfF8qy03RjR722HE0qWPd-WC5ZiSz4A
> .
@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:NP624914.RA4kMjSZHkrM3GtfF8qy03RjR722HE0qWPd-WC5ZiSz4A130_head
{
this:
np:hasAssertion
dgn-np:NP624914.RA4kMjSZHkrM3GtfF8qy03RjR722HE0qWPd-WC5ZiSz4A130_assertion
;
np:hasProvenance
dgn-np:NP624914.RA4kMjSZHkrM3GtfF8qy03RjR722HE0qWPd-WC5ZiSz4A130_provenance
;
np:hasPublicationInfo
dgn-np:NP624914.RA4kMjSZHkrM3GtfF8qy03RjR722HE0qWPd-WC5ZiSz4A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP624914.RA4kMjSZHkrM3GtfF8qy03RjR722HE0qWPd-WC5ZiSz4A130_assertion
a
np:Assertion
.
dgn-np:NP624914.RA4kMjSZHkrM3GtfF8qy03RjR722HE0qWPd-WC5ZiSz4A130_provenance
a
np:Provenance
.
dgn-np:NP624914.RA4kMjSZHkrM3GtfF8qy03RjR722HE0qWPd-WC5ZiSz4A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP624914.RA4kMjSZHkrM3GtfF8qy03RjR722HE0qWPd-WC5ZiSz4A130_assertion
{
miriam-gene:6648
a
ncit:C16612
.
lld:C0013384
a
ncit:C7057
.
dgn-gda:DGN75de5856cc02efdff19d794b47ebd9a1
sio:SIO_000628
miriam-gene:6648
,
lld:C0013384
;
a
sio:SIO_001121
.
}
dgn-np:NP624914.RA4kMjSZHkrM3GtfF8qy03RjR722HE0qWPd-WC5ZiSz4A130_provenance
{
dgn-np:NP624914.RA4kMjSZHkrM3GtfF8qy03RjR722HE0qWPd-WC5ZiSz4A130_assertion
dcterms:description
"[Chinese Han patients with schizophrenia were assessed for abnormal involuntary movements, and subgroups of 42 patients with persistent tardive dyskinesia and 59 consistently without dyskinesias were assessed for the DRD3 ser9gly and the MnSOD ala-9val polymorphisms.]. 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:12960753
;
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:NP624914.RA4kMjSZHkrM3GtfF8qy03RjR722HE0qWPd-WC5ZiSz4A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:17+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" .
}