@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ
> .
@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:NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_head
{
this:
np:hasAssertion
dgn-np:NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_assertion
;
np:hasProvenance
dgn-np:NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_assertion
a
np:Assertion
.
dgn-np:NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_provenance
a
np:Provenance
.
dgn-np:NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_assertion
{
miriam-gene:4015
a
ncit:C16612
.
lld:C0267244
a
ncit:C7057
.
dgn-gda:DGNc031acbb2af43a37803340c18f0a3b89
sio:SIO_000628
miriam-gene:4015
,
lld:C0267244
;
a
sio:SIO_001121
.
}
dgn-np:NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_provenance
{
dgn-np:NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_assertion
dcterms:description
"[The majority of genes identified by RDA showed nearly complete concordance with microarray results, and also led to the identification of some differentially expressed genes such as lysyl oxidase, copper transporter ATP7A, EphB6, RUNX2 and a variant of RUNX2.]. 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:16314837
;
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:NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:56+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" .
}