@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8
> .
@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:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_head
{
this:
np:hasAssertion
dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_assertion
;
np:hasProvenance
dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_provenance
;
np:hasPublicationInfo
dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_assertion
a
np:Assertion
.
dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_provenance
a
np:Provenance
.
dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0018213
a
ncit:C7057
.
dgn-gda:DGN1db687bf9bbb2c7fba2cca39342a7107
sio:SIO_000628
miriam-gene:7421
,
lld:C0018213
;
a
sio:SIO_001121
.
}
dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_provenance
{
dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_assertion
dcterms:description
"[This is the largest and most comprehensive study of the VDR gene in GD to date and these data suggest that these polymorphisms of the VDR gene do not contribute to GD susceptibility in the UK.]. 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:15104566
;
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:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:10+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" .
}