@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8
> .
@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:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_head
{
this:
np:hasAssertion
dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_assertion
;
np:hasProvenance
dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_provenance
;
np:hasPublicationInfo
dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_assertion
a
np:Assertion
.
dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_provenance
a
np:Provenance
.
dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_assertion
{
miriam-gene:5460
a
ncit:C16612
.
lld:C0855197
a
ncit:C7057
.
dgn-gda:DGN0bbd3be02abda7cd631e53123ab8c7ca
sio:SIO_000628
miriam-gene:5460
,
lld:C0855197
;
a
sio:SIO_001121
.
}
dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_provenance
{
dgn-np:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_assertion
dcterms:description
"[Failure to switch off OCT4 in GC perinatally can lead to development of carcinoma in situ (CIS), the precursor of testicular germ cell cancer (TGCC), for which there is no animal model.]. 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:23321215
;
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:NP842655.RAsi9LtPQIIHFLoumdEAxMkH0ZddpbggN1cWKgFWUgij8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:35+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" .
}