@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP51544.RAlgi2XtpNcT5VZovMyPV9ByXIWo0ZLWqFSihUZ0GFsaw
> .
@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:NP51544.RAlgi2XtpNcT5VZovMyPV9ByXIWo0ZLWqFSihUZ0GFsaw130_head
{
this:
np:hasAssertion
dgn-np:NP51544.RAlgi2XtpNcT5VZovMyPV9ByXIWo0ZLWqFSihUZ0GFsaw130_assertion
;
np:hasProvenance
dgn-np:NP51544.RAlgi2XtpNcT5VZovMyPV9ByXIWo0ZLWqFSihUZ0GFsaw130_provenance
;
np:hasPublicationInfo
dgn-np:NP51544.RAlgi2XtpNcT5VZovMyPV9ByXIWo0ZLWqFSihUZ0GFsaw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51544.RAlgi2XtpNcT5VZovMyPV9ByXIWo0ZLWqFSihUZ0GFsaw130_assertion
a
np:Assertion
.
dgn-np:NP51544.RAlgi2XtpNcT5VZovMyPV9ByXIWo0ZLWqFSihUZ0GFsaw130_provenance
a
np:Provenance
.
dgn-np:NP51544.RAlgi2XtpNcT5VZovMyPV9ByXIWo0ZLWqFSihUZ0GFsaw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51544.RAlgi2XtpNcT5VZovMyPV9ByXIWo0ZLWqFSihUZ0GFsaw130_assertion
{
miriam-gene:6531
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN7597da81ef489d77cc0090577b2f89ee
sio:SIO_000628
miriam-gene:6531
,
lld:C0036341
;
a
sio:SIO_001122
.
}
dgn-np:NP51544.RAlgi2XtpNcT5VZovMyPV9ByXIWo0ZLWqFSihUZ0GFsaw130_provenance
{
dgn-np:NP51544.RAlgi2XtpNcT5VZovMyPV9ByXIWo0ZLWqFSihUZ0GFsaw130_assertion
dcterms:description
"[Inherited or acquired dysfunction of the dopamine system is believed to underlie the core symptoms of schizophrenia, and there are some evidences that dopamine transporter activity may be altered in schizophrenic patients.]. 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:15380858
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP51544.RAlgi2XtpNcT5VZovMyPV9ByXIWo0ZLWqFSihUZ0GFsaw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}