@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP734313.RAAHIjJQCncIH3E6JvI_FdeAgmrORWGZ47c5rMC1XbXjg
> .
@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:NP734313.RAAHIjJQCncIH3E6JvI_FdeAgmrORWGZ47c5rMC1XbXjg130_head
{
this:
np:hasAssertion
dgn-np:NP734313.RAAHIjJQCncIH3E6JvI_FdeAgmrORWGZ47c5rMC1XbXjg130_assertion
;
np:hasProvenance
dgn-np:NP734313.RAAHIjJQCncIH3E6JvI_FdeAgmrORWGZ47c5rMC1XbXjg130_provenance
;
np:hasPublicationInfo
dgn-np:NP734313.RAAHIjJQCncIH3E6JvI_FdeAgmrORWGZ47c5rMC1XbXjg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP734313.RAAHIjJQCncIH3E6JvI_FdeAgmrORWGZ47c5rMC1XbXjg130_assertion
a
np:Assertion
.
dgn-np:NP734313.RAAHIjJQCncIH3E6JvI_FdeAgmrORWGZ47c5rMC1XbXjg130_provenance
a
np:Provenance
.
dgn-np:NP734313.RAAHIjJQCncIH3E6JvI_FdeAgmrORWGZ47c5rMC1XbXjg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP734313.RAAHIjJQCncIH3E6JvI_FdeAgmrORWGZ47c5rMC1XbXjg130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C0015672
a
ncit:C7057
.
dgn-gda:DGN6f99a9778da57dd8fa7b70950157a262
sio:SIO_000628
miriam-gene:1813
,
lld:C0015672
;
a
sio:SIO_001121
.
}
dgn-np:NP734313.RAAHIjJQCncIH3E6JvI_FdeAgmrORWGZ47c5rMC1XbXjg130_provenance
{
dgn-np:NP734313.RAAHIjJQCncIH3E6JvI_FdeAgmrORWGZ47c5rMC1XbXjg130_assertion
dcterms:description
"[Other genetic associations were also observed in men but not women, such as greater 'feel effects' and anger, and reduced fatigue, in the dopamine D2 receptor (DRD2 C957T single nucleotide polymorphism) TT versus CT or CC genotypes.]. 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:18690117
;
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:NP734313.RAAHIjJQCncIH3E6JvI_FdeAgmrORWGZ47c5rMC1XbXjg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:25+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" .
}