@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP290438.RATCkmLIx-XMbmwHSWrklM_JH7RUjPsCMrQX5lKBcU1Ks
> .
@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:NP290438.RATCkmLIx-XMbmwHSWrklM_JH7RUjPsCMrQX5lKBcU1Ks130_head
{
this:
np:hasAssertion
dgn-np:NP290438.RATCkmLIx-XMbmwHSWrklM_JH7RUjPsCMrQX5lKBcU1Ks130_assertion
;
np:hasProvenance
dgn-np:NP290438.RATCkmLIx-XMbmwHSWrklM_JH7RUjPsCMrQX5lKBcU1Ks130_provenance
;
np:hasPublicationInfo
dgn-np:NP290438.RATCkmLIx-XMbmwHSWrklM_JH7RUjPsCMrQX5lKBcU1Ks130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP290438.RATCkmLIx-XMbmwHSWrklM_JH7RUjPsCMrQX5lKBcU1Ks130_assertion
a
np:Assertion
.
dgn-np:NP290438.RATCkmLIx-XMbmwHSWrklM_JH7RUjPsCMrQX5lKBcU1Ks130_provenance
a
np:Provenance
.
dgn-np:NP290438.RATCkmLIx-XMbmwHSWrklM_JH7RUjPsCMrQX5lKBcU1Ks130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP290438.RATCkmLIx-XMbmwHSWrklM_JH7RUjPsCMrQX5lKBcU1Ks130_assertion
{
miriam-gene:3569
a
ncit:C16612
.
lld:C0029401
a
ncit:C7057
.
dgn-gda:DGN077916baef703e5deee7751fbb77a24a
sio:SIO_000628
miriam-gene:3569
,
lld:C0029401
;
a
sio:SIO_001121
.
}
dgn-np:NP290438.RATCkmLIx-XMbmwHSWrklM_JH7RUjPsCMrQX5lKBcU1Ks130_provenance
{
dgn-np:NP290438.RATCkmLIx-XMbmwHSWrklM_JH7RUjPsCMrQX5lKBcU1Ks130_assertion
dcterms:description
"[Analyzing 9 tag SNPs and 2 multi-marker tests (MMTs) in TNFSF11, 3 tag SNPs and 1 MMT in VCP and 8 tag SNPs in IL-6 in a population of 196 Belgian patients with sporadic PDB and 212 Belgian control individuals revealed that one VCP SNP (rs565070) turned out to be associated with PDB in this Belgian study population (p=5.5×10(-3)).]. 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:21501964
;
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:NP290438.RATCkmLIx-XMbmwHSWrklM_JH7RUjPsCMrQX5lKBcU1Ks130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:45+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" .
}