@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro
> .
@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:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_head
{
this:
np:hasAssertion
dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_assertion
;
np:hasProvenance
dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_provenance
;
np:hasPublicationInfo
dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_assertion
a
np:Assertion
.
dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_provenance
a
np:Provenance
.
dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_assertion
{
miriam-gene:159
a
ncit:C16612
.
lld:C0019348
a
ncit:C7057
.
dgn-gda:DGN46ac695a2c24f3c0a162b182839366dc
sio:SIO_000628
miriam-gene:159
,
lld:C0019348
;
a
sio:SIO_001121
.
}
dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_provenance
{
dgn-np:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_assertion
dcterms:description
"[Our findings suggest that distinct markers in IRF2 may be associated with AD and ADEH, which may depend upon ethnic ancestry, and genetic variants in IRF2 may contribute to an abnormal immune response to HSV.]. 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:22113474
;
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:NP812133.RAmzZCFXkUEd339HvVHAjV4YvSypz_FAJzUlg00RDIuro130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:18+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" .
}