@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP471644.RAAkC50hFYSkby3yRpH0A8LKKXyoMEd1RfCJsvAJnHCSc
> .
@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:NP471644.RAAkC50hFYSkby3yRpH0A8LKKXyoMEd1RfCJsvAJnHCSc130_head
{
this:
np:hasAssertion
dgn-np:NP471644.RAAkC50hFYSkby3yRpH0A8LKKXyoMEd1RfCJsvAJnHCSc130_assertion
;
np:hasProvenance
dgn-np:NP471644.RAAkC50hFYSkby3yRpH0A8LKKXyoMEd1RfCJsvAJnHCSc130_provenance
;
np:hasPublicationInfo
dgn-np:NP471644.RAAkC50hFYSkby3yRpH0A8LKKXyoMEd1RfCJsvAJnHCSc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP471644.RAAkC50hFYSkby3yRpH0A8LKKXyoMEd1RfCJsvAJnHCSc130_assertion
a
np:Assertion
.
dgn-np:NP471644.RAAkC50hFYSkby3yRpH0A8LKKXyoMEd1RfCJsvAJnHCSc130_provenance
a
np:Provenance
.
dgn-np:NP471644.RAAkC50hFYSkby3yRpH0A8LKKXyoMEd1RfCJsvAJnHCSc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP471644.RAAkC50hFYSkby3yRpH0A8LKKXyoMEd1RfCJsvAJnHCSc130_assertion
{
miriam-gene:2215
a
ncit:C16612
.
lld:C0004364
a
ncit:C7057
.
dgn-gda:DGNd7b63d1c0d7fe7be7626997fefa721b8
sio:SIO_000628
miriam-gene:2215
,
lld:C0004364
;
a
sio:SIO_001121
.
}
dgn-np:NP471644.RAAkC50hFYSkby3yRpH0A8LKKXyoMEd1RfCJsvAJnHCSc130_provenance
{
dgn-np:NP471644.RAAkC50hFYSkby3yRpH0A8LKKXyoMEd1RfCJsvAJnHCSc130_assertion
dcterms:description
"[Here, we determined the association between CNV in the gene encoding FCGR3B with the risk of developing autoimmune diseases and whether the observed associations are modified by the CNV in CCL3L1 (CC chemokine ligand 3-like 1), a gene encoding a potent chemokine.]. 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:19741716
;
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:NP471644.RAAkC50hFYSkby3yRpH0A8LKKXyoMEd1RfCJsvAJnHCSc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:42+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" .
}