@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP699829.RAJifnpj8dSedlJKkUNTuKzKqZT1EVv1UsE9qs6Wc4ILg
> .
@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:NP699829.RAJifnpj8dSedlJKkUNTuKzKqZT1EVv1UsE9qs6Wc4ILg130_head
{
this:
np:hasAssertion
dgn-np:NP699829.RAJifnpj8dSedlJKkUNTuKzKqZT1EVv1UsE9qs6Wc4ILg130_assertion
;
np:hasProvenance
dgn-np:NP699829.RAJifnpj8dSedlJKkUNTuKzKqZT1EVv1UsE9qs6Wc4ILg130_provenance
;
np:hasPublicationInfo
dgn-np:NP699829.RAJifnpj8dSedlJKkUNTuKzKqZT1EVv1UsE9qs6Wc4ILg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP699829.RAJifnpj8dSedlJKkUNTuKzKqZT1EVv1UsE9qs6Wc4ILg130_assertion
a
np:Assertion
.
dgn-np:NP699829.RAJifnpj8dSedlJKkUNTuKzKqZT1EVv1UsE9qs6Wc4ILg130_provenance
a
np:Provenance
.
dgn-np:NP699829.RAJifnpj8dSedlJKkUNTuKzKqZT1EVv1UsE9qs6Wc4ILg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP699829.RAJifnpj8dSedlJKkUNTuKzKqZT1EVv1UsE9qs6Wc4ILg130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C1704272
a
ncit:C7057
.
dgn-gda:DGN1915a700c20aff4d3e405b5943b086d8
sio:SIO_000628
miriam-gene:7421
,
lld:C1704272
;
a
sio:SIO_001121
.
}
dgn-np:NP699829.RAJifnpj8dSedlJKkUNTuKzKqZT1EVv1UsE9qs6Wc4ILg130_provenance
{
dgn-np:NP699829.RAJifnpj8dSedlJKkUNTuKzKqZT1EVv1UsE9qs6Wc4ILg130_assertion
dcterms:description
"[The association between CYP3A4 and VDR TaqI SNPs and the risk of developing PRCa have been investigated in this study by determining the variant genotype frequencies of both SNPs in 400 patients with BPH who have been followed clinically for a median of 11 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:12644831
;
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:NP699829.RAJifnpj8dSedlJKkUNTuKzKqZT1EVv1UsE9qs6Wc4ILg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:05+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" .
}