@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP922571.RApJVaLUWcRSGcRQVFZrFslvbs7Dcl26Oo0EzvtCBdTUU
> .
@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:NP922571.RApJVaLUWcRSGcRQVFZrFslvbs7Dcl26Oo0EzvtCBdTUU130_head
{
this:
np:hasAssertion
dgn-np:NP922571.RApJVaLUWcRSGcRQVFZrFslvbs7Dcl26Oo0EzvtCBdTUU130_assertion
;
np:hasProvenance
dgn-np:NP922571.RApJVaLUWcRSGcRQVFZrFslvbs7Dcl26Oo0EzvtCBdTUU130_provenance
;
np:hasPublicationInfo
dgn-np:NP922571.RApJVaLUWcRSGcRQVFZrFslvbs7Dcl26Oo0EzvtCBdTUU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP922571.RApJVaLUWcRSGcRQVFZrFslvbs7Dcl26Oo0EzvtCBdTUU130_assertion
a
np:Assertion
.
dgn-np:NP922571.RApJVaLUWcRSGcRQVFZrFslvbs7Dcl26Oo0EzvtCBdTUU130_provenance
a
np:Provenance
.
dgn-np:NP922571.RApJVaLUWcRSGcRQVFZrFslvbs7Dcl26Oo0EzvtCBdTUU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP922571.RApJVaLUWcRSGcRQVFZrFslvbs7Dcl26Oo0EzvtCBdTUU130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0686347
a
ncit:C7057
.
dgn-gda:DGNf24f38294e557920e12a1cb0b1d5682f
sio:SIO_000628
miriam-gene:348
,
lld:C0686347
;
a
sio:SIO_001121
.
}
dgn-np:NP922571.RApJVaLUWcRSGcRQVFZrFslvbs7Dcl26Oo0EzvtCBdTUU130_provenance
{
dgn-np:NP922571.RApJVaLUWcRSGcRQVFZrFslvbs7Dcl26Oo0EzvtCBdTUU130_assertion
dcterms:description
"[APOE genotype-specific risks of both tardive dyskinesia and Alzheimer's disease that vary across populations could be due to recruitment of patients or controls or could be due to modifying effects of differing genetic or environmental backgrounds.]. 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:16261623
;
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:NP922571.RApJVaLUWcRSGcRQVFZrFslvbs7Dcl26Oo0EzvtCBdTUU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:26+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" .
}