@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk
> .
@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:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_head
{
this:
np:hasAssertion
dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_assertion
;
np:hasProvenance
dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_provenance
;
np:hasPublicationInfo
dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_assertion
a
np:Assertion
.
dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_provenance
a
np:Provenance
.
dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_assertion
{
miriam-gene:196
a
ncit:C16612
.
lld:C0024299
a
ncit:C7057
.
dgn-gda:DGNb017c0828633ea6d20438ed72c7df85b
sio:SIO_000628
miriam-gene:196
,
lld:C0024299
;
a
sio:SIO_001122
.
}
dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_provenance
{
dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_assertion
dcterms:description
"[In this case-control study conducted in British Columbia, Canada, five single nucleotide polymorphisms (SNPs) of AHR were genotyped in 422 NHL cases and 459 controls to measure the association between individual SNPs, haplotypes, and risk of NHL.]. 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:19821039
;
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:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:36+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" .
}