@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP674067.RArlj8A6RvdAXQZ105WK7eJtloaIGBrvm3MXni6qG7by0
> .
@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:NP674067.RArlj8A6RvdAXQZ105WK7eJtloaIGBrvm3MXni6qG7by0130_head
{
this:
np:hasAssertion
dgn-np:NP674067.RArlj8A6RvdAXQZ105WK7eJtloaIGBrvm3MXni6qG7by0130_assertion
;
np:hasProvenance
dgn-np:NP674067.RArlj8A6RvdAXQZ105WK7eJtloaIGBrvm3MXni6qG7by0130_provenance
;
np:hasPublicationInfo
dgn-np:NP674067.RArlj8A6RvdAXQZ105WK7eJtloaIGBrvm3MXni6qG7by0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP674067.RArlj8A6RvdAXQZ105WK7eJtloaIGBrvm3MXni6qG7by0130_assertion
a
np:Assertion
.
dgn-np:NP674067.RArlj8A6RvdAXQZ105WK7eJtloaIGBrvm3MXni6qG7by0130_provenance
a
np:Provenance
.
dgn-np:NP674067.RArlj8A6RvdAXQZ105WK7eJtloaIGBrvm3MXni6qG7by0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP674067.RArlj8A6RvdAXQZ105WK7eJtloaIGBrvm3MXni6qG7by0130_assertion
{
miriam-gene:6657
a
ncit:C16612
.
lld:C0036631
a
ncit:C7057
.
dgn-gda:DGNb980c13c52fc4d7888794e0cd708bd38
sio:SIO_000628
miriam-gene:6657
,
lld:C0036631
;
a
sio:SIO_001121
.
}
dgn-np:NP674067.RArlj8A6RvdAXQZ105WK7eJtloaIGBrvm3MXni6qG7by0130_provenance
{
dgn-np:NP674067.RArlj8A6RvdAXQZ105WK7eJtloaIGBrvm3MXni6qG7by0130_assertion
dcterms:description
"[Here we demonstrate that SOX2 is absent in germ cells of human fetal gonads, and as expected carcinoma in situ (CIS), ie the precursor lesion of testicular germ cell tumours of adolescents and adults (TGCTs), and seminoma.]. 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:18348160
;
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:NP674067.RArlj8A6RvdAXQZ105WK7eJtloaIGBrvm3MXni6qG7by0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:47+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" .
}