@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP204863.RAz7gazE8b-iUi6mLA4pSEI_ZKN6b3-9me1-wkXhAabP0
> .
@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:NP204863.RAz7gazE8b-iUi6mLA4pSEI_ZKN6b3-9me1-wkXhAabP0130_head
{
this:
np:hasAssertion
dgn-np:NP204863.RAz7gazE8b-iUi6mLA4pSEI_ZKN6b3-9me1-wkXhAabP0130_assertion
;
np:hasProvenance
dgn-np:NP204863.RAz7gazE8b-iUi6mLA4pSEI_ZKN6b3-9me1-wkXhAabP0130_provenance
;
np:hasPublicationInfo
dgn-np:NP204863.RAz7gazE8b-iUi6mLA4pSEI_ZKN6b3-9me1-wkXhAabP0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP204863.RAz7gazE8b-iUi6mLA4pSEI_ZKN6b3-9me1-wkXhAabP0130_assertion
a
np:Assertion
.
dgn-np:NP204863.RAz7gazE8b-iUi6mLA4pSEI_ZKN6b3-9me1-wkXhAabP0130_provenance
a
np:Provenance
.
dgn-np:NP204863.RAz7gazE8b-iUi6mLA4pSEI_ZKN6b3-9me1-wkXhAabP0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP204863.RAz7gazE8b-iUi6mLA4pSEI_ZKN6b3-9me1-wkXhAabP0130_assertion
{
miriam-gene:51750
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGN18705083dd468caf444b870332632d9d
sio:SIO_000628
miriam-gene:51750
,
lld:C0017638
;
a
sio:SIO_001121
.
}
dgn-np:NP204863.RAz7gazE8b-iUi6mLA4pSEI_ZKN6b3-9me1-wkXhAabP0130_provenance
{
dgn-np:NP204863.RAz7gazE8b-iUi6mLA4pSEI_ZKN6b3-9me1-wkXhAabP0130_assertion
dcterms:description
"[In conclusion, as previously shown for glioma regardless of family history of brain tumours, rs6010620 (RTEL1) was associated with an increased risk of glioma when restricting to cases with family history of brain tumours.]. 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:23115063
;
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:NP204863.RAz7gazE8b-iUi6mLA4pSEI_ZKN6b3-9me1-wkXhAabP0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:53+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" .
}