@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP217746.RAMc5FUEMJ6FfOqWB360EW34PaWcbtZqe531_KHO8BLBc
> .
@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:NP217746.RAMc5FUEMJ6FfOqWB360EW34PaWcbtZqe531_KHO8BLBc130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP217746.RAMc5FUEMJ6FfOqWB360EW34PaWcbtZqe531_KHO8BLBc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP217746.RAMc5FUEMJ6FfOqWB360EW34PaWcbtZqe531_KHO8BLBc130_assertion
a
np:Assertion
.
dgn-np:NP217746.RAMc5FUEMJ6FfOqWB360EW34PaWcbtZqe531_KHO8BLBc130_provenance
a
np:Provenance
.
dgn-np:NP217746.RAMc5FUEMJ6FfOqWB360EW34PaWcbtZqe531_KHO8BLBc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP217746.RAMc5FUEMJ6FfOqWB360EW34PaWcbtZqe531_KHO8BLBc130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN40ea912ab37fb20eaaf9b8f26951b41b
sio:SIO_000628
miriam-gene:1813
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP217746.RAMc5FUEMJ6FfOqWB360EW34PaWcbtZqe531_KHO8BLBc130_provenance
{
dgn-np:NP217746.RAMc5FUEMJ6FfOqWB360EW34PaWcbtZqe531_KHO8BLBc130_assertion
dcterms:description
"[The altered hetero-dimerization that likely results from the lower expression of these genetic variants of D(1)R with D(2)R may be partially responsible for the association of both G198A and G1263A polymorphisms with the schizophrenia phenotype.]. 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:20081237
;
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:NP217746.RAMc5FUEMJ6FfOqWB360EW34PaWcbtZqe531_KHO8BLBc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:01+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
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"v2.1.0" .
}