@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP204447.RA42meUKAeqtlD7eVauZaMQ7Q4dEF4RLI_N7yoI3-xTSY
> .
@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:NP204447.RA42meUKAeqtlD7eVauZaMQ7Q4dEF4RLI_N7yoI3-xTSY130_head
{
this:
np:hasAssertion
dgn-np:NP204447.RA42meUKAeqtlD7eVauZaMQ7Q4dEF4RLI_N7yoI3-xTSY130_assertion
;
np:hasProvenance
dgn-np:NP204447.RA42meUKAeqtlD7eVauZaMQ7Q4dEF4RLI_N7yoI3-xTSY130_provenance
;
np:hasPublicationInfo
dgn-np:NP204447.RA42meUKAeqtlD7eVauZaMQ7Q4dEF4RLI_N7yoI3-xTSY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP204447.RA42meUKAeqtlD7eVauZaMQ7Q4dEF4RLI_N7yoI3-xTSY130_assertion
a
np:Assertion
.
dgn-np:NP204447.RA42meUKAeqtlD7eVauZaMQ7Q4dEF4RLI_N7yoI3-xTSY130_provenance
a
np:Provenance
.
dgn-np:NP204447.RA42meUKAeqtlD7eVauZaMQ7Q4dEF4RLI_N7yoI3-xTSY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP204447.RA42meUKAeqtlD7eVauZaMQ7Q4dEF4RLI_N7yoI3-xTSY130_assertion
{
miriam-gene:4683
a
ncit:C16612
.
lld:C2931456
a
ncit:C7057
.
dgn-gda:DGN423609579d90502fc3aa925cb860bd7e
sio:SIO_000628
miriam-gene:4683
,
lld:C2931456
;
a
sio:SIO_001121
.
}
dgn-np:NP204447.RA42meUKAeqtlD7eVauZaMQ7Q4dEF4RLI_N7yoI3-xTSY130_provenance
{
dgn-np:NP204447.RA42meUKAeqtlD7eVauZaMQ7Q4dEF4RLI_N7yoI3-xTSY130_assertion
dcterms:description
"[Our study did not reveal predisposition genes for hereditary prostate cancer as the founder mutations of the BRCA1 and NBS1 genes are rarely detected in Latvia, but showed the importance of evaluation risk individually as a positive family history of cancer was associated with the earlier onset of prostate cancer.]. 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:22186123
;
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:NP204447.RA42meUKAeqtlD7eVauZaMQ7Q4dEF4RLI_N7yoI3-xTSY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:52+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" .
}