@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP62766.RA1XK887Axtua6iJc6JaY5V1zGbt336ODBGuD8HeWsCLs
> .
@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:NP62766.RA1XK887Axtua6iJc6JaY5V1zGbt336ODBGuD8HeWsCLs130_head
{
this:
np:hasAssertion
dgn-np:NP62766.RA1XK887Axtua6iJc6JaY5V1zGbt336ODBGuD8HeWsCLs130_assertion
;
np:hasProvenance
dgn-np:NP62766.RA1XK887Axtua6iJc6JaY5V1zGbt336ODBGuD8HeWsCLs130_provenance
;
np:hasPublicationInfo
dgn-np:NP62766.RA1XK887Axtua6iJc6JaY5V1zGbt336ODBGuD8HeWsCLs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP62766.RA1XK887Axtua6iJc6JaY5V1zGbt336ODBGuD8HeWsCLs130_assertion
a
np:Assertion
.
dgn-np:NP62766.RA1XK887Axtua6iJc6JaY5V1zGbt336ODBGuD8HeWsCLs130_provenance
a
np:Provenance
.
dgn-np:NP62766.RA1XK887Axtua6iJc6JaY5V1zGbt336ODBGuD8HeWsCLs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP62766.RA1XK887Axtua6iJc6JaY5V1zGbt336ODBGuD8HeWsCLs130_assertion
{
miriam-gene:1815
a
ncit:C16612
.
lld:C0740858
a
ncit:C7057
.
dgn-gda:DGN42d669edd45add9ce4b409c26fbc993b
sio:SIO_000628
miriam-gene:1815
,
lld:C0740858
;
a
sio:SIO_001122
.
}
dgn-np:NP62766.RA1XK887Axtua6iJc6JaY5V1zGbt336ODBGuD8HeWsCLs130_provenance
{
dgn-np:NP62766.RA1XK887Axtua6iJc6JaY5V1zGbt336ODBGuD8HeWsCLs130_assertion
dcterms:description
"[Long forms of the DRD4 VNTR are more frequent in substance abusers, but there is no interaction with previously published data on these individuals analyzing the COMT gene. There is no difference in DRD3 allele frequencies in these samples. ]. 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:11054777
;
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:NP62766.RA1XK887Axtua6iJc6JaY5V1zGbt336ODBGuD8HeWsCLs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}