@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP437893.RAkJDkGjbVxmzTApNVhs7mkV2FBt8mlwsGt4_NO3z5XlU
> .
@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:NP437893.RAkJDkGjbVxmzTApNVhs7mkV2FBt8mlwsGt4_NO3z5XlU130_head
{
this:
np:hasAssertion
dgn-np:NP437893.RAkJDkGjbVxmzTApNVhs7mkV2FBt8mlwsGt4_NO3z5XlU130_assertion
;
np:hasProvenance
dgn-np:NP437893.RAkJDkGjbVxmzTApNVhs7mkV2FBt8mlwsGt4_NO3z5XlU130_provenance
;
np:hasPublicationInfo
dgn-np:NP437893.RAkJDkGjbVxmzTApNVhs7mkV2FBt8mlwsGt4_NO3z5XlU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP437893.RAkJDkGjbVxmzTApNVhs7mkV2FBt8mlwsGt4_NO3z5XlU130_assertion
a
np:Assertion
.
dgn-np:NP437893.RAkJDkGjbVxmzTApNVhs7mkV2FBt8mlwsGt4_NO3z5XlU130_provenance
a
np:Provenance
.
dgn-np:NP437893.RAkJDkGjbVxmzTApNVhs7mkV2FBt8mlwsGt4_NO3z5XlU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP437893.RAkJDkGjbVxmzTApNVhs7mkV2FBt8mlwsGt4_NO3z5XlU130_assertion
{
miriam-gene:6531
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGNe9ee57ee1b255517271ed2fb5312025e
sio:SIO_000628
miriam-gene:6531
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP437893.RAkJDkGjbVxmzTApNVhs7mkV2FBt8mlwsGt4_NO3z5XlU130_provenance
{
dgn-np:NP437893.RAkJDkGjbVxmzTApNVhs7mkV2FBt8mlwsGt4_NO3z5XlU130_assertion
dcterms:description
"[Furthermore, DAT mutant mice provided an opportunity to model in vivo conditions of extreme dopaminergic dysfunction that could be relevant for human disorders such as ADHD, schizophrenia, and Parkinson's disease and, thus, could serve as test systems for developing novel treatments for these and related disorders.]. 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:18057916
;
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:NP437893.RAkJDkGjbVxmzTApNVhs7mkV2FBt8mlwsGt4_NO3z5XlU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:19+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" .
}