@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708648.RAKZl9tyBMe8e0mW9SS0iXnvRlGorcE3_bhdiVpam2G5A
> .
@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:NP708648.RAKZl9tyBMe8e0mW9SS0iXnvRlGorcE3_bhdiVpam2G5A130_head
{
this:
np:hasAssertion
dgn-np:NP708648.RAKZl9tyBMe8e0mW9SS0iXnvRlGorcE3_bhdiVpam2G5A130_assertion
;
np:hasProvenance
dgn-np:NP708648.RAKZl9tyBMe8e0mW9SS0iXnvRlGorcE3_bhdiVpam2G5A130_provenance
;
np:hasPublicationInfo
dgn-np:NP708648.RAKZl9tyBMe8e0mW9SS0iXnvRlGorcE3_bhdiVpam2G5A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708648.RAKZl9tyBMe8e0mW9SS0iXnvRlGorcE3_bhdiVpam2G5A130_assertion
a
np:Assertion
.
dgn-np:NP708648.RAKZl9tyBMe8e0mW9SS0iXnvRlGorcE3_bhdiVpam2G5A130_provenance
a
np:Provenance
.
dgn-np:NP708648.RAKZl9tyBMe8e0mW9SS0iXnvRlGorcE3_bhdiVpam2G5A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708648.RAKZl9tyBMe8e0mW9SS0iXnvRlGorcE3_bhdiVpam2G5A130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGN93905f16f4ad0d6be878c3a14a2f45da
sio:SIO_000628
miriam-gene:7421
,
lld:C1140680
;
a
sio:SIO_001121
.
}
dgn-np:NP708648.RAKZl9tyBMe8e0mW9SS0iXnvRlGorcE3_bhdiVpam2G5A130_provenance
{
dgn-np:NP708648.RAKZl9tyBMe8e0mW9SS0iXnvRlGorcE3_bhdiVpam2G5A130_assertion
dcterms:description
"[The strength of the association between the VDR gene FokI polymorphism and ovarian cancer risk was estimated under the allelic (T vs. C), homozygous (TT vs. CC), additive (CT vs. CC), recessive (TT vs. CC + CT), and dominant (CT + TT vs. CC) gene models.]. 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:24078452
;
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:NP708648.RAKZl9tyBMe8e0mW9SS0iXnvRlGorcE3_bhdiVpam2G5A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}