@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP86813.RAEBxZaJtN2ZppWxvjA4VUv9hrEGziBEI53-7h-c9a5mg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP86813.RAEBxZaJtN2ZppWxvjA4VUv9hrEGziBEI53-7h-c9a5mg130_head
{
this:
np:hasAssertion
dgn-np:NP86813.RAEBxZaJtN2ZppWxvjA4VUv9hrEGziBEI53-7h-c9a5mg130_assertion
;
np:hasProvenance
dgn-np:NP86813.RAEBxZaJtN2ZppWxvjA4VUv9hrEGziBEI53-7h-c9a5mg130_provenance
;
np:hasPublicationInfo
dgn-np:NP86813.RAEBxZaJtN2ZppWxvjA4VUv9hrEGziBEI53-7h-c9a5mg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP86813.RAEBxZaJtN2ZppWxvjA4VUv9hrEGziBEI53-7h-c9a5mg130_assertion
a
np:Assertion
.
dgn-np:NP86813.RAEBxZaJtN2ZppWxvjA4VUv9hrEGziBEI53-7h-c9a5mg130_provenance
a
np:Provenance
.
dgn-np:NP86813.RAEBxZaJtN2ZppWxvjA4VUv9hrEGziBEI53-7h-c9a5mg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP86813.RAEBxZaJtN2ZppWxvjA4VUv9hrEGziBEI53-7h-c9a5mg130_assertion
{
miriam-gene:1401
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGN57d6758fdae05c36156d59d01bf10876
sio:SIO_000628
miriam-gene:1401
,
lld:C0242383
;
a
sio:SIO_001122
.
}
dgn-np:NP86813.RAEBxZaJtN2ZppWxvjA4VUv9hrEGziBEI53-7h-c9a5mg130_provenance
{
dgn-np:NP86813.RAEBxZaJtN2ZppWxvjA4VUv9hrEGziBEI53-7h-c9a5mg130_assertion
dcterms:description
"[We provide evidence that if elevated serum/plasma levels of CRP are associated with neovascular AMD, it is likely not due to genetic variation within CRP, but likely due to variations in some other genetic as well as epidemiological 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:18704199
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP86813.RAEBxZaJtN2ZppWxvjA4VUv9hrEGziBEI53-7h-c9a5mg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:28+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}