@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c
> .
@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:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_head
{
this:
np:hasAssertion
dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_assertion
;
np:hasProvenance
dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_provenance
;
np:hasPublicationInfo
dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_assertion
a
np:Assertion
.
dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_provenance
a
np:Provenance
.
dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0038525
a
ncit:C7057
.
dgn-gda:DGN299a83f895beab47ffc8a57cd9b32f1e
sio:SIO_000628
miriam-gene:348
,
lld:C0038525
;
a
sio:SIO_001122
.
}
dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_provenance
{
dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_assertion
dcterms:description
"[Presence of the APOE4 allele is associated with poorer response to traumatic brain injury and ischemic stroke, but the association between APOE genotype and outcome following aneurysmal subarachnoid hemorrhage (SAH) remains unclear.]. 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:19017669
;
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:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}