@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP704647.RAyVPOeXE86wngNEzWeeRvxelCL5vki9uPjyurO6vJmbE
> .
@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:NP704647.RAyVPOeXE86wngNEzWeeRvxelCL5vki9uPjyurO6vJmbE130_head
{
this:
np:hasAssertion
dgn-np:NP704647.RAyVPOeXE86wngNEzWeeRvxelCL5vki9uPjyurO6vJmbE130_assertion
;
np:hasProvenance
dgn-np:NP704647.RAyVPOeXE86wngNEzWeeRvxelCL5vki9uPjyurO6vJmbE130_provenance
;
np:hasPublicationInfo
dgn-np:NP704647.RAyVPOeXE86wngNEzWeeRvxelCL5vki9uPjyurO6vJmbE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP704647.RAyVPOeXE86wngNEzWeeRvxelCL5vki9uPjyurO6vJmbE130_assertion
a
np:Assertion
.
dgn-np:NP704647.RAyVPOeXE86wngNEzWeeRvxelCL5vki9uPjyurO6vJmbE130_provenance
a
np:Provenance
.
dgn-np:NP704647.RAyVPOeXE86wngNEzWeeRvxelCL5vki9uPjyurO6vJmbE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP704647.RAyVPOeXE86wngNEzWeeRvxelCL5vki9uPjyurO6vJmbE130_assertion
{
miriam-gene:5891
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN643f2a0ff6e2ac21580141d3ed7f6052
sio:SIO_000628
miriam-gene:5891
,
lld:C0027051
;
a
sio:SIO_001121
.
}
dgn-np:NP704647.RAyVPOeXE86wngNEzWeeRvxelCL5vki9uPjyurO6vJmbE130_provenance
{
dgn-np:NP704647.RAyVPOeXE86wngNEzWeeRvxelCL5vki9uPjyurO6vJmbE130_assertion
dcterms:description
"[This study is the first to investigate the role of RAGE polymorphisms on the susceptibility to develop the acute coronary events in the Italian population and identified this polymorphism as an age-related factor for MI development.]. 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:21208063
;
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:NP704647.RAyVPOeXE86wngNEzWeeRvxelCL5vki9uPjyurO6vJmbE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:08+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" .
}