@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP534166.RAPxH6pp5PrnvF1IcMej-IaVWVTmoRB3bzEeBTz_u7TB4
> .
@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:NP534166.RAPxH6pp5PrnvF1IcMej-IaVWVTmoRB3bzEeBTz_u7TB4130_head
{
this:
np:hasAssertion
dgn-np:NP534166.RAPxH6pp5PrnvF1IcMej-IaVWVTmoRB3bzEeBTz_u7TB4130_assertion
;
np:hasProvenance
dgn-np:NP534166.RAPxH6pp5PrnvF1IcMej-IaVWVTmoRB3bzEeBTz_u7TB4130_provenance
;
np:hasPublicationInfo
dgn-np:NP534166.RAPxH6pp5PrnvF1IcMej-IaVWVTmoRB3bzEeBTz_u7TB4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP534166.RAPxH6pp5PrnvF1IcMej-IaVWVTmoRB3bzEeBTz_u7TB4130_assertion
a
np:Assertion
.
dgn-np:NP534166.RAPxH6pp5PrnvF1IcMej-IaVWVTmoRB3bzEeBTz_u7TB4130_provenance
a
np:Provenance
.
dgn-np:NP534166.RAPxH6pp5PrnvF1IcMej-IaVWVTmoRB3bzEeBTz_u7TB4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP534166.RAPxH6pp5PrnvF1IcMej-IaVWVTmoRB3bzEeBTz_u7TB4130_assertion
{
miriam-gene:1861
a
ncit:C16612
.
lld:C2732473
a
ncit:C7057
.
dgn-gda:DGNabd8c0a4427aad2eecc5ba551a64414d
sio:SIO_000628
miriam-gene:1861
,
lld:C2732473
;
a
sio:SIO_001121
.
}
dgn-np:NP534166.RAPxH6pp5PrnvF1IcMej-IaVWVTmoRB3bzEeBTz_u7TB4130_provenance
{
dgn-np:NP534166.RAPxH6pp5PrnvF1IcMej-IaVWVTmoRB3bzEeBTz_u7TB4130_assertion
dcterms:description
"[The major conclusion that holds true in both populations is that, while DQ2 is an absolute requirement for the development of CD, the presence of an additional genetic factor within the MIC-Class I region confers an approximate 4-fold increased risk of the 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:12753669
;
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:NP534166.RAPxH6pp5PrnvF1IcMej-IaVWVTmoRB3bzEeBTz_u7TB4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:22+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" .
}