@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP635012.RAE4CDZI1LT_bV2ti0xxTyHNTJLQTjtFqkFKT5KwDLqdE
> .
@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:NP635012.RAE4CDZI1LT_bV2ti0xxTyHNTJLQTjtFqkFKT5KwDLqdE130_head
{
this:
np:hasAssertion
dgn-np:NP635012.RAE4CDZI1LT_bV2ti0xxTyHNTJLQTjtFqkFKT5KwDLqdE130_assertion
;
np:hasProvenance
dgn-np:NP635012.RAE4CDZI1LT_bV2ti0xxTyHNTJLQTjtFqkFKT5KwDLqdE130_provenance
;
np:hasPublicationInfo
dgn-np:NP635012.RAE4CDZI1LT_bV2ti0xxTyHNTJLQTjtFqkFKT5KwDLqdE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP635012.RAE4CDZI1LT_bV2ti0xxTyHNTJLQTjtFqkFKT5KwDLqdE130_assertion
a
np:Assertion
.
dgn-np:NP635012.RAE4CDZI1LT_bV2ti0xxTyHNTJLQTjtFqkFKT5KwDLqdE130_provenance
a
np:Provenance
.
dgn-np:NP635012.RAE4CDZI1LT_bV2ti0xxTyHNTJLQTjtFqkFKT5KwDLqdE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP635012.RAE4CDZI1LT_bV2ti0xxTyHNTJLQTjtFqkFKT5KwDLqdE130_assertion
{
miriam-gene:1814
a
ncit:C16612
.
lld:C0013384
a
ncit:C7057
.
dgn-gda:DGN0b13a8fe329aace6766fef42d110d1e9
sio:SIO_000628
miriam-gene:1814
,
lld:C0013384
;
a
sio:SIO_001121
.
}
dgn-np:NP635012.RAE4CDZI1LT_bV2ti0xxTyHNTJLQTjtFqkFKT5KwDLqdE130_provenance
{
dgn-np:NP635012.RAE4CDZI1LT_bV2ti0xxTyHNTJLQTjtFqkFKT5KwDLqdE130_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:NP635012.RAE4CDZI1LT_bV2ti0xxTyHNTJLQTjtFqkFKT5KwDLqdE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:23+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" .
}