@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP226284.RAv2U_lEaTQ9o8Qy8bIJS2zSnUYsUK6ht1o8-HOmKisOk
> .
@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:NP226284.RAv2U_lEaTQ9o8Qy8bIJS2zSnUYsUK6ht1o8-HOmKisOk130_head
{
this:
np:hasAssertion
dgn-np:NP226284.RAv2U_lEaTQ9o8Qy8bIJS2zSnUYsUK6ht1o8-HOmKisOk130_assertion
;
np:hasProvenance
dgn-np:NP226284.RAv2U_lEaTQ9o8Qy8bIJS2zSnUYsUK6ht1o8-HOmKisOk130_provenance
;
np:hasPublicationInfo
dgn-np:NP226284.RAv2U_lEaTQ9o8Qy8bIJS2zSnUYsUK6ht1o8-HOmKisOk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP226284.RAv2U_lEaTQ9o8Qy8bIJS2zSnUYsUK6ht1o8-HOmKisOk130_assertion
a
np:Assertion
.
dgn-np:NP226284.RAv2U_lEaTQ9o8Qy8bIJS2zSnUYsUK6ht1o8-HOmKisOk130_provenance
a
np:Provenance
.
dgn-np:NP226284.RAv2U_lEaTQ9o8Qy8bIJS2zSnUYsUK6ht1o8-HOmKisOk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP226284.RAv2U_lEaTQ9o8Qy8bIJS2zSnUYsUK6ht1o8-HOmKisOk130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0158252
a
ncit:C7057
.
dgn-gda:DGN823964d6b275cfe865a5d1ba973c8a12
sio:SIO_000628
miriam-gene:7421
,
lld:C0158252
;
a
sio:SIO_001121
.
}
dgn-np:NP226284.RAv2U_lEaTQ9o8Qy8bIJS2zSnUYsUK6ht1o8-HOmKisOk130_provenance
{
dgn-np:NP226284.RAv2U_lEaTQ9o8Qy8bIJS2zSnUYsUK6ht1o8-HOmKisOk130_assertion
dcterms:description
"[This meta-analysis suggested that the alleles with shorter VNTR length significantly increased the risk of IDD, while the VDR (TaqI, FokI, ApaI) gene polymorphisms were not significantly associated with the risk of IDD.]. 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:23209686
;
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:NP226284.RAv2U_lEaTQ9o8Qy8bIJS2zSnUYsUK6ht1o8-HOmKisOk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:05+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" .
}