@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP51540.RAilv3Zd05d45Sz7OIqBp-J0fbi7i4BvaeXMCwU370pFo
> .
@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:NP51540.RAilv3Zd05d45Sz7OIqBp-J0fbi7i4BvaeXMCwU370pFo130_head
{
this:
np:hasAssertion
dgn-np:NP51540.RAilv3Zd05d45Sz7OIqBp-J0fbi7i4BvaeXMCwU370pFo130_assertion
;
np:hasProvenance
dgn-np:NP51540.RAilv3Zd05d45Sz7OIqBp-J0fbi7i4BvaeXMCwU370pFo130_provenance
;
np:hasPublicationInfo
dgn-np:NP51540.RAilv3Zd05d45Sz7OIqBp-J0fbi7i4BvaeXMCwU370pFo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51540.RAilv3Zd05d45Sz7OIqBp-J0fbi7i4BvaeXMCwU370pFo130_assertion
a
np:Assertion
.
dgn-np:NP51540.RAilv3Zd05d45Sz7OIqBp-J0fbi7i4BvaeXMCwU370pFo130_provenance
a
np:Provenance
.
dgn-np:NP51540.RAilv3Zd05d45Sz7OIqBp-J0fbi7i4BvaeXMCwU370pFo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51540.RAilv3Zd05d45Sz7OIqBp-J0fbi7i4BvaeXMCwU370pFo130_assertion
{
miriam-gene:6531
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN1d95cd659675dca51ccee266d408717a
sio:SIO_000628
miriam-gene:6531
,
lld:C0036341
;
a
sio:SIO_001122
.
}
dgn-np:NP51540.RAilv3Zd05d45Sz7OIqBp-J0fbi7i4BvaeXMCwU370pFo130_provenance
{
dgn-np:NP51540.RAilv3Zd05d45Sz7OIqBp-J0fbi7i4BvaeXMCwU370pFo130_assertion
dcterms:description
"[Our objectives were (i) to examine epistasis between the DAT 3' UTR variable number of tandem repeats (VNTR) and COMT Val158Met polymorphisms on brain activation during executive function, and (ii) to then determine the extent to which such interaction is altered in schizophrenia.]. 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:19666577
;
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:NP51540.RAilv3Zd05d45Sz7OIqBp-J0fbi7i4BvaeXMCwU370pFo130_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" .
}