@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP810083.RAYHMLUjDkx9sUEucXRmovGhU5fRHblkKJN6BF1J0aa-0
> .
@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:NP810083.RAYHMLUjDkx9sUEucXRmovGhU5fRHblkKJN6BF1J0aa-0130_head
{
this:
np:hasAssertion
dgn-np:NP810083.RAYHMLUjDkx9sUEucXRmovGhU5fRHblkKJN6BF1J0aa-0130_assertion
;
np:hasProvenance
dgn-np:NP810083.RAYHMLUjDkx9sUEucXRmovGhU5fRHblkKJN6BF1J0aa-0130_provenance
;
np:hasPublicationInfo
dgn-np:NP810083.RAYHMLUjDkx9sUEucXRmovGhU5fRHblkKJN6BF1J0aa-0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP810083.RAYHMLUjDkx9sUEucXRmovGhU5fRHblkKJN6BF1J0aa-0130_assertion
a
np:Assertion
.
dgn-np:NP810083.RAYHMLUjDkx9sUEucXRmovGhU5fRHblkKJN6BF1J0aa-0130_provenance
a
np:Provenance
.
dgn-np:NP810083.RAYHMLUjDkx9sUEucXRmovGhU5fRHblkKJN6BF1J0aa-0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP810083.RAYHMLUjDkx9sUEucXRmovGhU5fRHblkKJN6BF1J0aa-0130_assertion
{
miriam-gene:3949
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGNc6ac8832f02fe22508673ffdbb40e7fc
sio:SIO_000628
miriam-gene:3949
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP810083.RAYHMLUjDkx9sUEucXRmovGhU5fRHblkKJN6BF1J0aa-0130_provenance
{
dgn-np:NP810083.RAYHMLUjDkx9sUEucXRmovGhU5fRHblkKJN6BF1J0aa-0130_assertion
dcterms:description
"[In this study, we examined the effect of intravenous administration of human umbilical cord blood (HUCB) mononuclear cells on the progression of atherosclerosis in male homozygous mice that had mutation in the low-density lipoprotein receptor (Ldlr(tm1Her) mutation mice).]. 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:18426084
;
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:NP810083.RAYHMLUjDkx9sUEucXRmovGhU5fRHblkKJN6BF1J0aa-0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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" .
}