@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM
> .
@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:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_head
{
this:
np:hasAssertion
dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_assertion
;
np:hasProvenance
dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_provenance
;
np:hasPublicationInfo
dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_assertion
a
np:Assertion
.
dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_provenance
a
np:Provenance
.
dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0033578
a
ncit:C7057
.
dgn-gda:DGN4d50e1a250f4fe38ed419cea5c83bc32
sio:SIO_000628
miriam-gene:7421
,
lld:C0033578
;
a
sio:SIO_001122
.
}
dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_provenance
{
dgn-np:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_assertion
dcterms:description
"[no correlation of VDR gene polymorphisms, as detected by Apal and Taql restriction fragments, in multiethnic Brazilian men (165 patients and 200 controls) with prostate cancer risk and parameters of disease severity was found ]. 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:15503828
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP104247.RAzLDpLqXmUlweSOpIFMqQbel0VlzLXUxE2ZnwUsKtHlM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:53+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" .
}