@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE
> .
@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:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_head
{
this:
np:hasAssertion
dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_assertion
;
np:hasProvenance
dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_provenance
;
np:hasPublicationInfo
dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_assertion
a
np:Assertion
.
dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_provenance
a
np:Provenance
.
dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN346630b5ff9c874a231e3073c5474dd7
sio:SIO_000628
miriam-gene:183
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_provenance
{
dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_assertion
dcterms:description
"[After informed consent was obtained, 63 patients (21 stroke subjects and 42 nonstroke control subjects matched according to age and sex) with SCD followed at local pediatric hematology clinics were genotyped to test the association of specific GT-repeat alleles of the AGT gene and occurrence of stroke.]. 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:11754397
;
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:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:45+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" .
}