@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP257238.RA8p9EwFfFj_A_B8ttGWKvSlCEsBT7rWhISDmePuk7KoM
> .
@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:NP257238.RA8p9EwFfFj_A_B8ttGWKvSlCEsBT7rWhISDmePuk7KoM130_head
{
this:
np:hasAssertion
dgn-np:NP257238.RA8p9EwFfFj_A_B8ttGWKvSlCEsBT7rWhISDmePuk7KoM130_assertion
;
np:hasProvenance
dgn-np:NP257238.RA8p9EwFfFj_A_B8ttGWKvSlCEsBT7rWhISDmePuk7KoM130_provenance
;
np:hasPublicationInfo
dgn-np:NP257238.RA8p9EwFfFj_A_B8ttGWKvSlCEsBT7rWhISDmePuk7KoM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP257238.RA8p9EwFfFj_A_B8ttGWKvSlCEsBT7rWhISDmePuk7KoM130_assertion
a
np:Assertion
.
dgn-np:NP257238.RA8p9EwFfFj_A_B8ttGWKvSlCEsBT7rWhISDmePuk7KoM130_provenance
a
np:Provenance
.
dgn-np:NP257238.RA8p9EwFfFj_A_B8ttGWKvSlCEsBT7rWhISDmePuk7KoM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP257238.RA8p9EwFfFj_A_B8ttGWKvSlCEsBT7rWhISDmePuk7KoM130_assertion
{
miriam-gene:3117
a
ncit:C16612
.
lld:C0007570
a
ncit:C7057
.
dgn-gda:DGNe8813a4229b8f57d0ec129445aa10909
sio:SIO_000628
miriam-gene:3117
,
lld:C0007570
;
a
sio:SIO_001121
.
}
dgn-np:NP257238.RA8p9EwFfFj_A_B8ttGWKvSlCEsBT7rWhISDmePuk7KoM130_provenance
{
dgn-np:NP257238.RA8p9EwFfFj_A_B8ttGWKvSlCEsBT7rWhISDmePuk7KoM130_assertion
dcterms:description
"[HLA-DQA1 and DQB1 molecular typing was performed in 218 adult CD patients (169 with uncomplicated CD, 27 with complicated CD, and 22 with potential CD) and 224 healthy stem cell donors.]. 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:21694611
;
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:NP257238.RA8p9EwFfFj_A_B8ttGWKvSlCEsBT7rWhISDmePuk7KoM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:23+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" .
}