@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_assertion
;
np:hasProvenance
dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_provenance
;
np:hasPublicationInfo
dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_assertion
a
np:Assertion
.
dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_provenance
a
np:Provenance
.
dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C0149654
a
ncit:C7057
.
dgn-gda:DGN07f71c3e406bebef2e3a06d61adbb9a1
sio:SIO_000628
miriam-gene:1813
,
lld:C0149654
;
a
sio:SIO_001121
.
}
dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_provenance
{
dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_assertion
dcterms:description
"[Further, interaction effects were found between the DRD2 TaqIA polymorphism and conduct disorder (trend level) as well as A1+ status and impulsivity, such that adolescents who were carriers of the A1 allele, and had conduct disorder or impulsive behavior, reported higher levels of problematic alcohol use than those who were non-carriers (A2/A2 or A1-).]. 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:19344737
;
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:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:46+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" .
}