@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP563641.RAM_A3skNUCmseFSE9-0Kk6b2j399CaVUwDLG77G2fISc
> .
@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:NP563641.RAM_A3skNUCmseFSE9-0Kk6b2j399CaVUwDLG77G2fISc130_head
{
this:
np:hasAssertion
dgn-np:NP563641.RAM_A3skNUCmseFSE9-0Kk6b2j399CaVUwDLG77G2fISc130_assertion
;
np:hasProvenance
dgn-np:NP563641.RAM_A3skNUCmseFSE9-0Kk6b2j399CaVUwDLG77G2fISc130_provenance
;
np:hasPublicationInfo
dgn-np:NP563641.RAM_A3skNUCmseFSE9-0Kk6b2j399CaVUwDLG77G2fISc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP563641.RAM_A3skNUCmseFSE9-0Kk6b2j399CaVUwDLG77G2fISc130_assertion
a
np:Assertion
.
dgn-np:NP563641.RAM_A3skNUCmseFSE9-0Kk6b2j399CaVUwDLG77G2fISc130_provenance
a
np:Provenance
.
dgn-np:NP563641.RAM_A3skNUCmseFSE9-0Kk6b2j399CaVUwDLG77G2fISc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP563641.RAM_A3skNUCmseFSE9-0Kk6b2j399CaVUwDLG77G2fISc130_assertion
{
miriam-gene:5891
a
ncit:C16612
.
lld:C0020456
a
ncit:C7057
.
dgn-gda:DGNbcea1bc1edeacfaf9ec60a1d0dc39894
sio:SIO_000628
miriam-gene:5891
,
lld:C0020456
;
a
sio:SIO_001121
.
}
dgn-np:NP563641.RAM_A3skNUCmseFSE9-0Kk6b2j399CaVUwDLG77G2fISc130_provenance
{
dgn-np:NP563641.RAM_A3skNUCmseFSE9-0Kk6b2j399CaVUwDLG77G2fISc130_assertion
dcterms:description
"[Finally, recent data tracking RAGE in the clinic suggest that levels of soluble RAGEs and polymorphisms in the gene encoding RAGE may hold promise for the identification of patients who are vulnerable to the complications of diabetes and/or are receptive to therapeutic interventions designed to prevent and reverse the damage inflicted by chronic hyperglycemia, irrespective of its etiology.]. 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:22211895
;
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:NP563641.RAM_A3skNUCmseFSE9-0Kk6b2j399CaVUwDLG77G2fISc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}