@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP335906.RAraGWPags8CT-Sim6cn8DwIWVS32QOfeLV_J8kQ7Lrdk
> .
@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:NP335906.RAraGWPags8CT-Sim6cn8DwIWVS32QOfeLV_J8kQ7Lrdk130_head
{
this:
np:hasAssertion
dgn-np:NP335906.RAraGWPags8CT-Sim6cn8DwIWVS32QOfeLV_J8kQ7Lrdk130_assertion
;
np:hasProvenance
dgn-np:NP335906.RAraGWPags8CT-Sim6cn8DwIWVS32QOfeLV_J8kQ7Lrdk130_provenance
;
np:hasPublicationInfo
dgn-np:NP335906.RAraGWPags8CT-Sim6cn8DwIWVS32QOfeLV_J8kQ7Lrdk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP335906.RAraGWPags8CT-Sim6cn8DwIWVS32QOfeLV_J8kQ7Lrdk130_assertion
a
np:Assertion
.
dgn-np:NP335906.RAraGWPags8CT-Sim6cn8DwIWVS32QOfeLV_J8kQ7Lrdk130_provenance
a
np:Provenance
.
dgn-np:NP335906.RAraGWPags8CT-Sim6cn8DwIWVS32QOfeLV_J8kQ7Lrdk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP335906.RAraGWPags8CT-Sim6cn8DwIWVS32QOfeLV_J8kQ7Lrdk130_assertion
{
miriam-gene:1401
a
ncit:C16612
.
lld:C0024437
a
ncit:C7057
.
dgn-gda:DGN53228b55910e8c80e122b7a17e913eba
sio:SIO_000628
miriam-gene:1401
,
lld:C0024437
;
a
sio:SIO_001121
.
}
dgn-np:NP335906.RAraGWPags8CT-Sim6cn8DwIWVS32QOfeLV_J8kQ7Lrdk130_provenance
{
dgn-np:NP335906.RAraGWPags8CT-Sim6cn8DwIWVS32QOfeLV_J8kQ7Lrdk130_assertion
dcterms:description
"[No statistically significant association was detected between any of the nine common variants in CRP and neovascular AMD when considering disease status alone or when controlling for smoking exposure, BMI, diabetes, or CFH genotype.]. 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: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:NP335906.RAraGWPags8CT-Sim6cn8DwIWVS32QOfeLV_J8kQ7Lrdk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:17+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" .
}