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http://rdf.disgenet.org/nanopublications.trig#NP371796.RAQLEJgmF5JOBH0UO8emRWLeyLyN-6CG3ir-I4EuerzGg
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP371796.RAQLEJgmF5JOBH0UO8emRWLeyLyN-6CG3ir-I4EuerzGg130_assertion
;
np:hasProvenance
dgn-np:NP371796.RAQLEJgmF5JOBH0UO8emRWLeyLyN-6CG3ir-I4EuerzGg130_provenance
;
np:hasPublicationInfo
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;
a
np:Nanopublication
.
dgn-np:NP371796.RAQLEJgmF5JOBH0UO8emRWLeyLyN-6CG3ir-I4EuerzGg130_assertion
a
np:Assertion
.
dgn-np:NP371796.RAQLEJgmF5JOBH0UO8emRWLeyLyN-6CG3ir-I4EuerzGg130_provenance
a
np:Provenance
.
dgn-np:NP371796.RAQLEJgmF5JOBH0UO8emRWLeyLyN-6CG3ir-I4EuerzGg130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:8618
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGNae5a9d09c72c3a4ea3901951d691c1ed
sio:SIO_000628
miriam-gene:8618
,
lld:C0376358
;
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.
}
dgn-np:NP371796.RAQLEJgmF5JOBH0UO8emRWLeyLyN-6CG3ir-I4EuerzGg130_provenance
{
dgn-np:NP371796.RAQLEJgmF5JOBH0UO8emRWLeyLyN-6CG3ir-I4EuerzGg130_assertion
dcterms:description
"[Suggestive associations were further confirmed using single-nucleotide polymorphisms (SNPs) that tagged the CNVs of interest in an additional 2895 aggressive and 3094 nonaggressive cases, including those from the remaining case subjects of the JHH study (JHH2), the NCI Cancer Genetic Markers of Susceptibility (CGEMS) Study, and the CAncer of the Prostate in Sweden (CAPS) Study.]. 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:21551127
;
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:NP371796.RAQLEJgmF5JOBH0UO8emRWLeyLyN-6CG3ir-I4EuerzGg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:38+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
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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pav:version
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}