@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP598705.RAV_Ayje5EVJaTxxdwK9K5de9dFG8W7yrIfGviWGqSfHw
> .
@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:NP598705.RAV_Ayje5EVJaTxxdwK9K5de9dFG8W7yrIfGviWGqSfHw130_head
{
this:
np:hasAssertion
dgn-np:NP598705.RAV_Ayje5EVJaTxxdwK9K5de9dFG8W7yrIfGviWGqSfHw130_assertion
;
np:hasProvenance
dgn-np:NP598705.RAV_Ayje5EVJaTxxdwK9K5de9dFG8W7yrIfGviWGqSfHw130_provenance
;
np:hasPublicationInfo
dgn-np:NP598705.RAV_Ayje5EVJaTxxdwK9K5de9dFG8W7yrIfGviWGqSfHw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP598705.RAV_Ayje5EVJaTxxdwK9K5de9dFG8W7yrIfGviWGqSfHw130_assertion
a
np:Assertion
.
dgn-np:NP598705.RAV_Ayje5EVJaTxxdwK9K5de9dFG8W7yrIfGviWGqSfHw130_provenance
a
np:Provenance
.
dgn-np:NP598705.RAV_Ayje5EVJaTxxdwK9K5de9dFG8W7yrIfGviWGqSfHw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP598705.RAV_Ayje5EVJaTxxdwK9K5de9dFG8W7yrIfGviWGqSfHw130_assertion
{
miriam-gene:6582
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGN65bc15e4b22ed78fc8e427a6b63309aa
sio:SIO_000628
miriam-gene:6582
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP598705.RAV_Ayje5EVJaTxxdwK9K5de9dFG8W7yrIfGviWGqSfHw130_provenance
{
dgn-np:NP598705.RAV_Ayje5EVJaTxxdwK9K5de9dFG8W7yrIfGviWGqSfHw130_assertion
dcterms:description
"[We conclude that the expression pattern of OCT2, SSX2-4, and SAGE1 supports the origin of SS from spermatogonia and provides new evidence for heterogeneity of this tumour, potentially linked either to the cellular origin of SS or to partial differentiation during tumour progression, including a hitherto unknown OCT2-positive variant of the tumour likely derived from A(dark) spermatogonia.]. 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:21706474
;
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:NP598705.RAV_Ayje5EVJaTxxdwK9K5de9dFG8W7yrIfGviWGqSfHw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:59+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" .
}