@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP244817.RADMbvxaWgyuLu-qJK6RUYBUJeZOO0fVSXqd63bDYBsK0
> .
@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:NP244817.RADMbvxaWgyuLu-qJK6RUYBUJeZOO0fVSXqd63bDYBsK0130_head
{
this:
np:hasAssertion
dgn-np:NP244817.RADMbvxaWgyuLu-qJK6RUYBUJeZOO0fVSXqd63bDYBsK0130_assertion
;
np:hasProvenance
dgn-np:NP244817.RADMbvxaWgyuLu-qJK6RUYBUJeZOO0fVSXqd63bDYBsK0130_provenance
;
np:hasPublicationInfo
dgn-np:NP244817.RADMbvxaWgyuLu-qJK6RUYBUJeZOO0fVSXqd63bDYBsK0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP244817.RADMbvxaWgyuLu-qJK6RUYBUJeZOO0fVSXqd63bDYBsK0130_assertion
a
np:Assertion
.
dgn-np:NP244817.RADMbvxaWgyuLu-qJK6RUYBUJeZOO0fVSXqd63bDYBsK0130_provenance
a
np:Provenance
.
dgn-np:NP244817.RADMbvxaWgyuLu-qJK6RUYBUJeZOO0fVSXqd63bDYBsK0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP244817.RADMbvxaWgyuLu-qJK6RUYBUJeZOO0fVSXqd63bDYBsK0130_assertion
{
miriam-gene:1814
a
ncit:C16612
.
lld:C0871189
a
ncit:C7057
.
dgn-gda:DGN4cc03665e65e0b96084b25982a4094ed
sio:SIO_000628
miriam-gene:1814
,
lld:C0871189
;
a
sio:SIO_001121
.
}
dgn-np:NP244817.RADMbvxaWgyuLu-qJK6RUYBUJeZOO0fVSXqd63bDYBsK0130_provenance
{
dgn-np:NP244817.RADMbvxaWgyuLu-qJK6RUYBUJeZOO0fVSXqd63bDYBsK0130_assertion
dcterms:description
"[We assessed relationships between genotypes/alleles of the DRD3 BalI polymorphism and the presence or absence of psychotic symptoms (delusions, hallucinations) in AD patients during the month prior to interview and at any stage during the dementia.]. 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:15342129
;
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:NP244817.RADMbvxaWgyuLu-qJK6RUYBUJeZOO0fVSXqd63bDYBsK0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:17+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" .
}