@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP775712.RAXua2VvXtv3jCCdHr0r1-KgbR8I3rIwE91cb3WQFoPj8
> .
@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:NP775712.RAXua2VvXtv3jCCdHr0r1-KgbR8I3rIwE91cb3WQFoPj8130_head
{
this:
np:hasAssertion
dgn-np:NP775712.RAXua2VvXtv3jCCdHr0r1-KgbR8I3rIwE91cb3WQFoPj8130_assertion
;
np:hasProvenance
dgn-np:NP775712.RAXua2VvXtv3jCCdHr0r1-KgbR8I3rIwE91cb3WQFoPj8130_provenance
;
np:hasPublicationInfo
dgn-np:NP775712.RAXua2VvXtv3jCCdHr0r1-KgbR8I3rIwE91cb3WQFoPj8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP775712.RAXua2VvXtv3jCCdHr0r1-KgbR8I3rIwE91cb3WQFoPj8130_assertion
a
np:Assertion
.
dgn-np:NP775712.RAXua2VvXtv3jCCdHr0r1-KgbR8I3rIwE91cb3WQFoPj8130_provenance
a
np:Provenance
.
dgn-np:NP775712.RAXua2VvXtv3jCCdHr0r1-KgbR8I3rIwE91cb3WQFoPj8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP775712.RAXua2VvXtv3jCCdHr0r1-KgbR8I3rIwE91cb3WQFoPj8130_assertion
{
miriam-gene:5175
a
ncit:C16612
.
lld:C0018133
a
ncit:C7057
.
dgn-gda:DGN755144035985853b7e48f341e723dc93
sio:SIO_000628
miriam-gene:5175
,
lld:C0018133
;
a
sio:SIO_001121
.
}
dgn-np:NP775712.RAXua2VvXtv3jCCdHr0r1-KgbR8I3rIwE91cb3WQFoPj8130_provenance
{
dgn-np:NP775712.RAXua2VvXtv3jCCdHr0r1-KgbR8I3rIwE91cb3WQFoPj8130_assertion
dcterms:description
"[Among the transplant recipients, 71 percent of those with acute GVHD had CD31 genotypes that were not identical to the donor's genotype, as compared with 22 percent of the recipients without GVHD (P = 0.004).]. 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:8532023
;
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:NP775712.RAXua2VvXtv3jCCdHr0r1-KgbR8I3rIwE91cb3WQFoPj8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:50+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" .
}