@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU
> .
@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:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_head
{
this:
np:hasAssertion
dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_assertion
;
np:hasProvenance
dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_provenance
;
np:hasPublicationInfo
dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_assertion
a
np:Assertion
.
dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_provenance
a
np:Provenance
.
dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_assertion
{
miriam-gene:84627
a
ncit:C16612
.
lld:C0266539
a
ncit:C7057
.
dgn-gda:DGN38e95f8e0420235b7b7fb52c908df2df
sio:SIO_000628
miriam-gene:84627
,
lld:C0266539
;
a
sio:SIO_001121
.
}
dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_provenance
{
dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_assertion
dcterms:description
"[Our findings suggest that in addition to rare variants in ZNF469 underlying CCT variation in BCS patients, more common variants near this gene may contribute to CCT variation in the general population.]. 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:20485516
;
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:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:45+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" .
}