@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP643798.RAqHHWTzR1Ml1COaPHwYp0hxdKRHtjHf3yxw95vEevO-o
> .
@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:NP643798.RAqHHWTzR1Ml1COaPHwYp0hxdKRHtjHf3yxw95vEevO-o130_head
{
this:
np:hasAssertion
dgn-np:NP643798.RAqHHWTzR1Ml1COaPHwYp0hxdKRHtjHf3yxw95vEevO-o130_assertion
;
np:hasProvenance
dgn-np:NP643798.RAqHHWTzR1Ml1COaPHwYp0hxdKRHtjHf3yxw95vEevO-o130_provenance
;
np:hasPublicationInfo
dgn-np:NP643798.RAqHHWTzR1Ml1COaPHwYp0hxdKRHtjHf3yxw95vEevO-o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP643798.RAqHHWTzR1Ml1COaPHwYp0hxdKRHtjHf3yxw95vEevO-o130_assertion
a
np:Assertion
.
dgn-np:NP643798.RAqHHWTzR1Ml1COaPHwYp0hxdKRHtjHf3yxw95vEevO-o130_provenance
a
np:Provenance
.
dgn-np:NP643798.RAqHHWTzR1Ml1COaPHwYp0hxdKRHtjHf3yxw95vEevO-o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP643798.RAqHHWTzR1Ml1COaPHwYp0hxdKRHtjHf3yxw95vEevO-o130_assertion
{
miriam-gene:929
a
ncit:C16612
.
lld:C0151317
a
ncit:C7057
.
dgn-gda:DGN1c59c793ed939015dec6100ed2ee8601
sio:SIO_000628
miriam-gene:929
,
lld:C0151317
;
a
sio:SIO_001121
.
}
dgn-np:NP643798.RAqHHWTzR1Ml1COaPHwYp0hxdKRHtjHf3yxw95vEevO-o130_provenance
{
dgn-np:NP643798.RAqHHWTzR1Ml1COaPHwYp0hxdKRHtjHf3yxw95vEevO-o130_assertion
dcterms:description
"[Because atherosclerosis is an inflammatory process apparently modulated by chronic infections, we studied the effect of single nucleotide polymorphisms (SNPs) in TLR4 and CD14 on the extent of clinically relevant atherosclerosis in patients with peripheral arterial disease (PAD).]. 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:16890863
;
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:NP643798.RAqHHWTzR1Ml1COaPHwYp0hxdKRHtjHf3yxw95vEevO-o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:28+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: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" .
}