@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP821222.RAcXapi-gGHqkD-fBlkNxqncVkggM7RwKZSRabPhhVGhs
> .
@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:NP821222.RAcXapi-gGHqkD-fBlkNxqncVkggM7RwKZSRabPhhVGhs130_head
{
this:
np:hasAssertion
dgn-np:NP821222.RAcXapi-gGHqkD-fBlkNxqncVkggM7RwKZSRabPhhVGhs130_assertion
;
np:hasProvenance
dgn-np:NP821222.RAcXapi-gGHqkD-fBlkNxqncVkggM7RwKZSRabPhhVGhs130_provenance
;
np:hasPublicationInfo
dgn-np:NP821222.RAcXapi-gGHqkD-fBlkNxqncVkggM7RwKZSRabPhhVGhs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP821222.RAcXapi-gGHqkD-fBlkNxqncVkggM7RwKZSRabPhhVGhs130_assertion
a
np:Assertion
.
dgn-np:NP821222.RAcXapi-gGHqkD-fBlkNxqncVkggM7RwKZSRabPhhVGhs130_provenance
a
np:Provenance
.
dgn-np:NP821222.RAcXapi-gGHqkD-fBlkNxqncVkggM7RwKZSRabPhhVGhs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP821222.RAcXapi-gGHqkD-fBlkNxqncVkggM7RwKZSRabPhhVGhs130_assertion
{
miriam-gene:3459
a
ncit:C16612
.
lld:C0155877
a
ncit:C7057
.
dgn-gda:DGN1c4606bf2dc38f17ffc5c487f3aed4f0
sio:SIO_000628
miriam-gene:3459
,
lld:C0155877
;
a
sio:SIO_001121
.
}
dgn-np:NP821222.RAcXapi-gGHqkD-fBlkNxqncVkggM7RwKZSRabPhhVGhs130_provenance
{
dgn-np:NP821222.RAcXapi-gGHqkD-fBlkNxqncVkggM7RwKZSRabPhhVGhs130_assertion
dcterms:description
"[For example, significant associations between markers in certain candidate genes (eg, STAT6, ADRB2, and IFNGR1) for traits such as high total IgE levels observed in resistance to extracellular parasitic disease in one population and atopic asthma in another supports the common disease/common variant model for disease.]. 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:16461122
;
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:NP821222.RAcXapi-gGHqkD-fBlkNxqncVkggM7RwKZSRabPhhVGhs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:23+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" .
}