@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP51600.RAATJlSszHv-S00RAXnGi_KiZnSJgtnldE92ur6LLeDW0
> .
@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:NP51600.RAATJlSszHv-S00RAXnGi_KiZnSJgtnldE92ur6LLeDW0130_head
{
this:
np:hasAssertion
dgn-np:NP51600.RAATJlSszHv-S00RAXnGi_KiZnSJgtnldE92ur6LLeDW0130_assertion
;
np:hasProvenance
dgn-np:NP51600.RAATJlSszHv-S00RAXnGi_KiZnSJgtnldE92ur6LLeDW0130_provenance
;
np:hasPublicationInfo
dgn-np:NP51600.RAATJlSszHv-S00RAXnGi_KiZnSJgtnldE92ur6LLeDW0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51600.RAATJlSszHv-S00RAXnGi_KiZnSJgtnldE92ur6LLeDW0130_assertion
a
np:Assertion
.
dgn-np:NP51600.RAATJlSszHv-S00RAXnGi_KiZnSJgtnldE92ur6LLeDW0130_provenance
a
np:Provenance
.
dgn-np:NP51600.RAATJlSszHv-S00RAXnGi_KiZnSJgtnldE92ur6LLeDW0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51600.RAATJlSszHv-S00RAXnGi_KiZnSJgtnldE92ur6LLeDW0130_assertion
{
miriam-gene:6530
a
ncit:C16612
.
lld:C1263846
a
ncit:C7057
.
dgn-gda:DGNb70cdebe84caef9c8a28f86a42f55c72
sio:SIO_000628
miriam-gene:6530
,
lld:C1263846
;
a
sio:SIO_001122
.
}
dgn-np:NP51600.RAATJlSszHv-S00RAXnGi_KiZnSJgtnldE92ur6LLeDW0130_provenance
{
dgn-np:NP51600.RAATJlSszHv-S00RAXnGi_KiZnSJgtnldE92ur6LLeDW0130_assertion
dcterms:description
"[ These findings suggest an association between the G1287A polymorphism of the norepinephrine transporter gene and variation in methylphenidate response. Further work is needed to confirm this finding and to assess its generalization to other ethnic groups.]. 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:15322419
;
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:NP51600.RAATJlSszHv-S00RAXnGi_KiZnSJgtnldE92ur6LLeDW0130_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" .
}