@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP837268.RAIzH7PRSkd5oyVIriw1nLGs9arPOMiLmdjlPnkMsKRog
> .
@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:NP837268.RAIzH7PRSkd5oyVIriw1nLGs9arPOMiLmdjlPnkMsKRog130_head
{
this:
np:hasAssertion
dgn-np:NP837268.RAIzH7PRSkd5oyVIriw1nLGs9arPOMiLmdjlPnkMsKRog130_assertion
;
np:hasProvenance
dgn-np:NP837268.RAIzH7PRSkd5oyVIriw1nLGs9arPOMiLmdjlPnkMsKRog130_provenance
;
np:hasPublicationInfo
dgn-np:NP837268.RAIzH7PRSkd5oyVIriw1nLGs9arPOMiLmdjlPnkMsKRog130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP837268.RAIzH7PRSkd5oyVIriw1nLGs9arPOMiLmdjlPnkMsKRog130_assertion
a
np:Assertion
.
dgn-np:NP837268.RAIzH7PRSkd5oyVIriw1nLGs9arPOMiLmdjlPnkMsKRog130_provenance
a
np:Provenance
.
dgn-np:NP837268.RAIzH7PRSkd5oyVIriw1nLGs9arPOMiLmdjlPnkMsKRog130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP837268.RAIzH7PRSkd5oyVIriw1nLGs9arPOMiLmdjlPnkMsKRog130_assertion
{
miriam-gene:3484
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN445a07b6b5a0a5b583a8aebbe588beac
sio:SIO_000628
miriam-gene:3484
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP837268.RAIzH7PRSkd5oyVIriw1nLGs9arPOMiLmdjlPnkMsKRog130_provenance
{
dgn-np:NP837268.RAIzH7PRSkd5oyVIriw1nLGs9arPOMiLmdjlPnkMsKRog130_assertion
dcterms:description
"[Eleven haplotype tagging SNPs and two single SNPs in the IGFBP1, IGFBP3, and IGFALS genes were genotyped within the CAncer Prostate in Sweden (CAPS) study including 2,774 cases and 1,736 controls.]. 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:19455605
;
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:NP837268.RAIzH7PRSkd5oyVIriw1nLGs9arPOMiLmdjlPnkMsKRog130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:32+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" .
}