@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP562807.RAs1Jsa2uMO9IhpNLaNtM6GLW0tGMe4YRyCxz8uYsuw7Q
> .
@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:NP562807.RAs1Jsa2uMO9IhpNLaNtM6GLW0tGMe4YRyCxz8uYsuw7Q130_head
{
this:
np:hasAssertion
dgn-np:NP562807.RAs1Jsa2uMO9IhpNLaNtM6GLW0tGMe4YRyCxz8uYsuw7Q130_assertion
;
np:hasProvenance
dgn-np:NP562807.RAs1Jsa2uMO9IhpNLaNtM6GLW0tGMe4YRyCxz8uYsuw7Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP562807.RAs1Jsa2uMO9IhpNLaNtM6GLW0tGMe4YRyCxz8uYsuw7Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP562807.RAs1Jsa2uMO9IhpNLaNtM6GLW0tGMe4YRyCxz8uYsuw7Q130_assertion
a
np:Assertion
.
dgn-np:NP562807.RAs1Jsa2uMO9IhpNLaNtM6GLW0tGMe4YRyCxz8uYsuw7Q130_provenance
a
np:Provenance
.
dgn-np:NP562807.RAs1Jsa2uMO9IhpNLaNtM6GLW0tGMe4YRyCxz8uYsuw7Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP562807.RAs1Jsa2uMO9IhpNLaNtM6GLW0tGMe4YRyCxz8uYsuw7Q130_assertion
{
miriam-gene:11200
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN84c8900fda04fb381d998cb2efcf0195
sio:SIO_000628
miriam-gene:11200
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP562807.RAs1Jsa2uMO9IhpNLaNtM6GLW0tGMe4YRyCxz8uYsuw7Q130_provenance
{
dgn-np:NP562807.RAs1Jsa2uMO9IhpNLaNtM6GLW0tGMe4YRyCxz8uYsuw7Q130_assertion
dcterms:description
"[We screened for the CHEK2*1100delC variant in 419 men diagnosed with prostate cancer in southern Sweden, 145 of whom were sporadic cases that were divided into two subgroups depending on whether they were diagnosed before (n=64) or after (n=81) the age of 55 years.]. 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:16452051
;
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:NP562807.RAs1Jsa2uMO9IhpNLaNtM6GLW0tGMe4YRyCxz8uYsuw7Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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" .
}