@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP770995.RA6qauxQZCvl0NwQVvPdoQpMcJXN1Dkf4z_3FyIrPTghA
> .
@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:NP770995.RA6qauxQZCvl0NwQVvPdoQpMcJXN1Dkf4z_3FyIrPTghA130_head
{
this:
np:hasAssertion
dgn-np:NP770995.RA6qauxQZCvl0NwQVvPdoQpMcJXN1Dkf4z_3FyIrPTghA130_assertion
;
np:hasProvenance
dgn-np:NP770995.RA6qauxQZCvl0NwQVvPdoQpMcJXN1Dkf4z_3FyIrPTghA130_provenance
;
np:hasPublicationInfo
dgn-np:NP770995.RA6qauxQZCvl0NwQVvPdoQpMcJXN1Dkf4z_3FyIrPTghA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP770995.RA6qauxQZCvl0NwQVvPdoQpMcJXN1Dkf4z_3FyIrPTghA130_assertion
a
np:Assertion
.
dgn-np:NP770995.RA6qauxQZCvl0NwQVvPdoQpMcJXN1Dkf4z_3FyIrPTghA130_provenance
a
np:Provenance
.
dgn-np:NP770995.RA6qauxQZCvl0NwQVvPdoQpMcJXN1Dkf4z_3FyIrPTghA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP770995.RA6qauxQZCvl0NwQVvPdoQpMcJXN1Dkf4z_3FyIrPTghA130_assertion
{
miriam-gene:860
a
ncit:C16612
.
lld:C0585442
a
ncit:C7057
.
dgn-gda:DGNb132d592f8352002d843ff5ce32ac439
sio:SIO_000628
miriam-gene:860
,
lld:C0585442
;
a
sio:SIO_001121
.
}
dgn-np:NP770995.RA6qauxQZCvl0NwQVvPdoQpMcJXN1Dkf4z_3FyIrPTghA130_provenance
{
dgn-np:NP770995.RA6qauxQZCvl0NwQVvPdoQpMcJXN1Dkf4z_3FyIrPTghA130_assertion
dcterms:description
"[Our analyses show that the RUNX2 interactome may be constitutively activated in osteosarcoma, and that the downstream intracellular pathways are strongly associated with the regulation of osteoblast differentiation and control of cell cycle and apoptosis in osteosarcoma.]. 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:19286668
;
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:NP770995.RA6qauxQZCvl0NwQVvPdoQpMcJXN1Dkf4z_3FyIrPTghA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:46+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" .
}