@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP62986.RAPfIy_5Nq23xbKMNaaJKuILDFixZfpguRuDn_z3a8pFw
> .
@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:NP62986.RAPfIy_5Nq23xbKMNaaJKuILDFixZfpguRuDn_z3a8pFw130_head
{
this:
np:hasAssertion
dgn-np:NP62986.RAPfIy_5Nq23xbKMNaaJKuILDFixZfpguRuDn_z3a8pFw130_assertion
;
np:hasProvenance
dgn-np:NP62986.RAPfIy_5Nq23xbKMNaaJKuILDFixZfpguRuDn_z3a8pFw130_provenance
;
np:hasPublicationInfo
dgn-np:NP62986.RAPfIy_5Nq23xbKMNaaJKuILDFixZfpguRuDn_z3a8pFw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP62986.RAPfIy_5Nq23xbKMNaaJKuILDFixZfpguRuDn_z3a8pFw130_assertion
a
np:Assertion
.
dgn-np:NP62986.RAPfIy_5Nq23xbKMNaaJKuILDFixZfpguRuDn_z3a8pFw130_provenance
a
np:Provenance
.
dgn-np:NP62986.RAPfIy_5Nq23xbKMNaaJKuILDFixZfpguRuDn_z3a8pFw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP62986.RAPfIy_5Nq23xbKMNaaJKuILDFixZfpguRuDn_z3a8pFw130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0451641
a
ncit:C7057
.
dgn-gda:DGN60fa74fed4e9b56c559f1190f3cb974d
sio:SIO_000628
miriam-gene:7421
,
lld:C0451641
;
a
sio:SIO_001122
.
}
dgn-np:NP62986.RAPfIy_5Nq23xbKMNaaJKuILDFixZfpguRuDn_z3a8pFw130_provenance
{
dgn-np:NP62986.RAPfIy_5Nq23xbKMNaaJKuILDFixZfpguRuDn_z3a8pFw130_assertion
dcterms:description
"[The VDR FokI polymorphism might be important in the clinical presentation of patients with calcium urolithiasis, especially for the frequency of stone episodes and age at first onset, although it is not associated with the formation of stones.]. 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:17419705
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP62986.RAPfIy_5Nq23xbKMNaaJKuILDFixZfpguRuDn_z3a8pFw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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" .
}