@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP55896.RAZwhJrPvNQjzXJGX2xsbCqxJzUTAi7bQTm9uycdUlsE8
> .
@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:NP55896.RAZwhJrPvNQjzXJGX2xsbCqxJzUTAi7bQTm9uycdUlsE8130_head
{
this:
np:hasAssertion
dgn-np:NP55896.RAZwhJrPvNQjzXJGX2xsbCqxJzUTAi7bQTm9uycdUlsE8130_assertion
;
np:hasProvenance
dgn-np:NP55896.RAZwhJrPvNQjzXJGX2xsbCqxJzUTAi7bQTm9uycdUlsE8130_provenance
;
np:hasPublicationInfo
dgn-np:NP55896.RAZwhJrPvNQjzXJGX2xsbCqxJzUTAi7bQTm9uycdUlsE8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55896.RAZwhJrPvNQjzXJGX2xsbCqxJzUTAi7bQTm9uycdUlsE8130_assertion
a
np:Assertion
.
dgn-np:NP55896.RAZwhJrPvNQjzXJGX2xsbCqxJzUTAi7bQTm9uycdUlsE8130_provenance
a
np:Provenance
.
dgn-np:NP55896.RAZwhJrPvNQjzXJGX2xsbCqxJzUTAi7bQTm9uycdUlsE8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55896.RAZwhJrPvNQjzXJGX2xsbCqxJzUTAi7bQTm9uycdUlsE8130_assertion
{
miriam-gene:1524
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN806ad93693cb62340e0722ec635f18ff
sio:SIO_000628
miriam-gene:1524
,
lld:C0007222
;
a
sio:SIO_001122
.
}
dgn-np:NP55896.RAZwhJrPvNQjzXJGX2xsbCqxJzUTAi7bQTm9uycdUlsE8130_provenance
{
dgn-np:NP55896.RAZwhJrPvNQjzXJGX2xsbCqxJzUTAi7bQTm9uycdUlsE8130_assertion
dcterms:description
"[ The rare CX3CR1 alleles were associated with an increased risk of BI and with reduced frequency of cardiovascular history. We propose that the extra adhesion of monocytes observed in individuals carrying rare alleles of CX3CR1 may favor mechanisms leadin]. 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:15681302
;
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:NP55896.RAZwhJrPvNQjzXJGX2xsbCqxJzUTAi7bQTm9uycdUlsE8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:10+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" .
}