@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP594909.RA785MlM8ERRK0fWEFbU6Ov8MtCiv_baF222TePbTc5yQ
> .
@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:NP594909.RA785MlM8ERRK0fWEFbU6Ov8MtCiv_baF222TePbTc5yQ130_head
{
this:
np:hasAssertion
dgn-np:NP594909.RA785MlM8ERRK0fWEFbU6Ov8MtCiv_baF222TePbTc5yQ130_assertion
;
np:hasProvenance
dgn-np:NP594909.RA785MlM8ERRK0fWEFbU6Ov8MtCiv_baF222TePbTc5yQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP594909.RA785MlM8ERRK0fWEFbU6Ov8MtCiv_baF222TePbTc5yQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP594909.RA785MlM8ERRK0fWEFbU6Ov8MtCiv_baF222TePbTc5yQ130_assertion
a
np:Assertion
.
dgn-np:NP594909.RA785MlM8ERRK0fWEFbU6Ov8MtCiv_baF222TePbTc5yQ130_provenance
a
np:Provenance
.
dgn-np:NP594909.RA785MlM8ERRK0fWEFbU6Ov8MtCiv_baF222TePbTc5yQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP594909.RA785MlM8ERRK0fWEFbU6Ov8MtCiv_baF222TePbTc5yQ130_assertion
{
miriam-gene:1440
a
ncit:C16612
.
lld:C0042373
a
ncit:C7057
.
dgn-gda:DGNa7ade0b3cb273dc55dc686473925edca
sio:SIO_000628
miriam-gene:1440
,
lld:C0042373
;
a
sio:SIO_001121
.
}
dgn-np:NP594909.RA785MlM8ERRK0fWEFbU6Ov8MtCiv_baF222TePbTc5yQ130_provenance
{
dgn-np:NP594909.RA785MlM8ERRK0fWEFbU6Ov8MtCiv_baF222TePbTc5yQ130_assertion
dcterms:description
"[This paper discusses why previous studies with EPC transplantation or mobilization with G-CSF have had negative results and proposes the use of Cobalt and Hydralazine to enhance EPC function to overcome the dysfunctional EPC phenotype that is seen in patients with vascular disease or cardiovascular risk factors.]. 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:18473772
;
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:NP594909.RA785MlM8ERRK0fWEFbU6Ov8MtCiv_baF222TePbTc5yQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:57+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" .
}