@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4
> .
@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 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:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_head
{
this:
np:hasAssertion
dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_assertion
;
np:hasProvenance
dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_provenance
;
np:hasPublicationInfo
dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_assertion
a
np:Assertion
.
dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_provenance
a
np:Provenance
.
dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_assertion
{
miriam-gene:3358
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN3bad21d4e52a362ffaaa0ec672b8f9e7
sio:SIO_000628
miriam-gene:3358
,
lld:C0036341
;
a
sio:SIO_001122
.
}
dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_provenance
{
dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_assertion
dct:description
"[The D2 polymorphism was found not to be significantly associated with baseline levels or changes in total PANSS in these patients. The D3 genotype is associated with the change in total PANSS (p<0.01), an effect reflecting positive and general (each p<0.0]. 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:15695058
;
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:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:26+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}