@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP56999.RAt2Q7kqs2pKbC6jLoLLkHOD7rKhS5SG7iekg2R9Wn1hQ
> .
@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:NP56999.RAt2Q7kqs2pKbC6jLoLLkHOD7rKhS5SG7iekg2R9Wn1hQ130_head
{
this:
np:hasAssertion
dgn-np:NP56999.RAt2Q7kqs2pKbC6jLoLLkHOD7rKhS5SG7iekg2R9Wn1hQ130_assertion
;
np:hasProvenance
dgn-np:NP56999.RAt2Q7kqs2pKbC6jLoLLkHOD7rKhS5SG7iekg2R9Wn1hQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP56999.RAt2Q7kqs2pKbC6jLoLLkHOD7rKhS5SG7iekg2R9Wn1hQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP56999.RAt2Q7kqs2pKbC6jLoLLkHOD7rKhS5SG7iekg2R9Wn1hQ130_assertion
a
np:Assertion
.
dgn-np:NP56999.RAt2Q7kqs2pKbC6jLoLLkHOD7rKhS5SG7iekg2R9Wn1hQ130_provenance
a
np:Provenance
.
dgn-np:NP56999.RAt2Q7kqs2pKbC6jLoLLkHOD7rKhS5SG7iekg2R9Wn1hQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP56999.RAt2Q7kqs2pKbC6jLoLLkHOD7rKhS5SG7iekg2R9Wn1hQ130_assertion
{
miriam-gene:3459
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGNcfc33946c42051c8bb44c455c2e9a696
sio:SIO_000628
miriam-gene:3459
,
lld:C0004096
;
a
sio:SIO_001122
.
}
dgn-np:NP56999.RAt2Q7kqs2pKbC6jLoLLkHOD7rKhS5SG7iekg2R9Wn1hQ130_provenance
{
dgn-np:NP56999.RAt2Q7kqs2pKbC6jLoLLkHOD7rKhS5SG7iekg2R9Wn1hQ130_assertion
dcterms:description
"[We investigated the association of IFNG (CA repeat polymorphism within the first intron), IRF1 (GT repeat polymorphism within the intron 7), IFNGR1 (Val 14 Met), and IFNGR2 (Gln 64 Arg) gene polymorphisms with atopic asthma in the Japanese child population.]. 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:11240951
;
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:NP56999.RAt2Q7kqs2pKbC6jLoLLkHOD7rKhS5SG7iekg2R9Wn1hQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:26+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" .
}