@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg
> .
@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:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_head
{
this:
np:hasAssertion
dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_assertion
;
np:hasProvenance
dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_provenance
;
np:hasPublicationInfo
dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_assertion
a
np:Assertion
.
dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_provenance
a
np:Provenance
.
dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_assertion
{
miriam-gene:118429
a
ncit:C16612
.
lld:C0220620
a
ncit:C7057
.
dgn-gda:DGN997194e832c6eb63e903757cff6fd0c7
sio:SIO_000628
miriam-gene:118429
,
lld:C0220620
;
a
sio:SIO_001121
.
}
dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_provenance
{
dgn-np:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_assertion
dcterms:description
"[We have performed in situ hybridization (ISH) studies on paraffin sections and on isolated nuclei of 13 pediatric GCT with particular emphasis on those chromosome abnormalities that are common in adult GCT.]. 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:7529045
;
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:NP282250.RA8GU8w_bffbThhovL0zyiRmuNtktPSR6WizHdQpLNvHg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:39+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" .
}