@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP502107.RAdN2Lume-0Zs0tur9THMZAGYSNDtm1PccVtBDBC2hCZQ
> .
@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:NP502107.RAdN2Lume-0Zs0tur9THMZAGYSNDtm1PccVtBDBC2hCZQ130_head
{
this:
np:hasAssertion
dgn-np:NP502107.RAdN2Lume-0Zs0tur9THMZAGYSNDtm1PccVtBDBC2hCZQ130_assertion
;
np:hasProvenance
dgn-np:NP502107.RAdN2Lume-0Zs0tur9THMZAGYSNDtm1PccVtBDBC2hCZQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP502107.RAdN2Lume-0Zs0tur9THMZAGYSNDtm1PccVtBDBC2hCZQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP502107.RAdN2Lume-0Zs0tur9THMZAGYSNDtm1PccVtBDBC2hCZQ130_assertion
a
np:Assertion
.
dgn-np:NP502107.RAdN2Lume-0Zs0tur9THMZAGYSNDtm1PccVtBDBC2hCZQ130_provenance
a
np:Provenance
.
dgn-np:NP502107.RAdN2Lume-0Zs0tur9THMZAGYSNDtm1PccVtBDBC2hCZQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP502107.RAdN2Lume-0Zs0tur9THMZAGYSNDtm1PccVtBDBC2hCZQ130_assertion
{
miriam-gene:3123
a
ncit:C16612
.
lld:C0856825
a
ncit:C7057
.
dgn-gda:DGN8f7ace62f27729f4fa0bc4deea002446
sio:SIO_000628
miriam-gene:3123
,
lld:C0856825
;
a
sio:SIO_001121
.
}
dgn-np:NP502107.RAdN2Lume-0Zs0tur9THMZAGYSNDtm1PccVtBDBC2hCZQ130_provenance
{
dgn-np:NP502107.RAdN2Lume-0Zs0tur9THMZAGYSNDtm1PccVtBDBC2hCZQ130_assertion
dcterms:description
"[Disparities in class II HLA alleles of the DRB1, DQA1, DQB1, DPA1, and DPB1 loci were not identified as significant risk factors for acute GVHD or death in the multivariate analysis.]. 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:9780337
;
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:NP502107.RAdN2Lume-0Zs0tur9THMZAGYSNDtm1PccVtBDBC2hCZQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:59+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" .
}