@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP316129.RAveZNTZqUGvSExjTlVsdRsUEshoj1lnu0aHUmEK2XmxA
> .
@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:NP316129.RAveZNTZqUGvSExjTlVsdRsUEshoj1lnu0aHUmEK2XmxA130_head
{
this:
np:hasAssertion
dgn-np:NP316129.RAveZNTZqUGvSExjTlVsdRsUEshoj1lnu0aHUmEK2XmxA130_assertion
;
np:hasProvenance
dgn-np:NP316129.RAveZNTZqUGvSExjTlVsdRsUEshoj1lnu0aHUmEK2XmxA130_provenance
;
np:hasPublicationInfo
dgn-np:NP316129.RAveZNTZqUGvSExjTlVsdRsUEshoj1lnu0aHUmEK2XmxA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP316129.RAveZNTZqUGvSExjTlVsdRsUEshoj1lnu0aHUmEK2XmxA130_assertion
a
np:Assertion
.
dgn-np:NP316129.RAveZNTZqUGvSExjTlVsdRsUEshoj1lnu0aHUmEK2XmxA130_provenance
a
np:Provenance
.
dgn-np:NP316129.RAveZNTZqUGvSExjTlVsdRsUEshoj1lnu0aHUmEK2XmxA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP316129.RAveZNTZqUGvSExjTlVsdRsUEshoj1lnu0aHUmEK2XmxA130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGNbe37e0007396ba0436fad370d43f6aad
sio:SIO_000628
miriam-gene:3126
,
lld:C0010346
;
a
sio:SIO_001121
.
}
dgn-np:NP316129.RAveZNTZqUGvSExjTlVsdRsUEshoj1lnu0aHUmEK2XmxA130_provenance
{
dgn-np:NP316129.RAveZNTZqUGvSExjTlVsdRsUEshoj1lnu0aHUmEK2XmxA130_assertion
dcterms:description
"[Previous studies have suggested that susceptibility to Crohn's disease (CD) is associated with the histocompatibility complex (HLA) class II alleles DR1, DQ5, and DR13 in the Caucasian population, DR7 in the French and German populations, and DR4 and DQ4 in the Japanese 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:10833064
;
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:NP316129.RAveZNTZqUGvSExjTlVsdRsUEshoj1lnu0aHUmEK2XmxA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:01+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" .
}