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http://rdf.disgenet.org/nanopublications.trig#NP805829.RAOavhilRrYFZ5lKlBfDXQDHmSeyFwik5i-OOO1muOc88
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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{
this:
np:hasAssertion
dgn-np:NP805829.RAOavhilRrYFZ5lKlBfDXQDHmSeyFwik5i-OOO1muOc88130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP805829.RAOavhilRrYFZ5lKlBfDXQDHmSeyFwik5i-OOO1muOc88130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP805829.RAOavhilRrYFZ5lKlBfDXQDHmSeyFwik5i-OOO1muOc88130_assertion
a
np:Assertion
.
dgn-np:NP805829.RAOavhilRrYFZ5lKlBfDXQDHmSeyFwik5i-OOO1muOc88130_provenance
a
np:Provenance
.
dgn-np:NP805829.RAOavhilRrYFZ5lKlBfDXQDHmSeyFwik5i-OOO1muOc88130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:1813
a
ncit:C16612
.
lld:C1510586
a
ncit:C7057
.
dgn-gda:DGN136d5134bfce7112e0f6628eb8421aad
sio:SIO_000628
miriam-gene:1813
,
lld:C1510586
;
a
sio:SIO_001121
.
}
dgn-np:NP805829.RAOavhilRrYFZ5lKlBfDXQDHmSeyFwik5i-OOO1muOc88130_provenance
{
dgn-np:NP805829.RAOavhilRrYFZ5lKlBfDXQDHmSeyFwik5i-OOO1muOc88130_assertion
dcterms:description
"[To investigate the effect of the Taq1A variant in the Dopamine D2 receptor gene (DRD2) and common functional genetic variants in the cytochrome P450 2D6 gene (CYP2D6) on prolactin levels in risperidone-treated boys with autism spectrum disorders and disruptive behavior disorders.]. 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:23851570
;
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:NP805829.RAOavhilRrYFZ5lKlBfDXQDHmSeyFwik5i-OOO1muOc88130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:14+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
;
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<
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> , <
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> , <
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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"v2.1.0" .
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