@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0
> .
@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:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_head
{
this:
np:hasAssertion
dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_assertion
;
np:hasProvenance
dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_provenance
;
np:hasPublicationInfo
dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_assertion
a
np:Assertion
.
dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_provenance
a
np:Provenance
.
dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_assertion
{
miriam-gene:5460
a
ncit:C16612
.
lld:C0007099
a
ncit:C7057
.
dgn-gda:DGNe0e51e9efdaf25ada8bea46d2be52131
sio:SIO_000628
miriam-gene:5460
,
lld:C0007099
;
a
sio:SIO_001121
.
}
dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_provenance
{
dgn-np:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_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:NP753249.RAPbxZbzG7CL6bT_H79VrSHrlXo1FFH4yqVVHzRdcoaW0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}