@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP339047.RAqBcneqhENtizWUUSDmG-e3wIynliGpkoqDVXfdJldw0
> .
@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:NP339047.RAqBcneqhENtizWUUSDmG-e3wIynliGpkoqDVXfdJldw0130_head
{
this:
np:hasAssertion
dgn-np:NP339047.RAqBcneqhENtizWUUSDmG-e3wIynliGpkoqDVXfdJldw0130_assertion
;
np:hasProvenance
dgn-np:NP339047.RAqBcneqhENtizWUUSDmG-e3wIynliGpkoqDVXfdJldw0130_provenance
;
np:hasPublicationInfo
dgn-np:NP339047.RAqBcneqhENtizWUUSDmG-e3wIynliGpkoqDVXfdJldw0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP339047.RAqBcneqhENtizWUUSDmG-e3wIynliGpkoqDVXfdJldw0130_assertion
a
np:Assertion
.
dgn-np:NP339047.RAqBcneqhENtizWUUSDmG-e3wIynliGpkoqDVXfdJldw0130_provenance
a
np:Provenance
.
dgn-np:NP339047.RAqBcneqhENtizWUUSDmG-e3wIynliGpkoqDVXfdJldw0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP339047.RAqBcneqhENtizWUUSDmG-e3wIynliGpkoqDVXfdJldw0130_assertion
{
miriam-gene:6598
a
ncit:C16612
.
lld:C2985524
a
ncit:C7057
.
dgn-gda:DGNb005264c76f95aa17580628e10e4248a
sio:SIO_000628
miriam-gene:6598
,
lld:C2985524
;
a
sio:SIO_001121
.
}
dgn-np:NP339047.RAqBcneqhENtizWUUSDmG-e3wIynliGpkoqDVXfdJldw0130_provenance
{
dgn-np:NP339047.RAqBcneqhENtizWUUSDmG-e3wIynliGpkoqDVXfdJldw0130_assertion
dcterms:description
"[This is supported by the occurence of choroid plexus carcinomas (CPC) in the setting of families with rhabdoid predisposition syndrome (RPS), (19) caused by germ line inactivation of the INI1 gene.]. 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:12946029
;
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:NP339047.RAqBcneqhENtizWUUSDmG-e3wIynliGpkoqDVXfdJldw0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:19+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" .
}