@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP876263.RAXTZidu6vxFrvnOrFEHIO4BeWQz52K79U6fj9c-8nbNA
> .
@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:NP876263.RAXTZidu6vxFrvnOrFEHIO4BeWQz52K79U6fj9c-8nbNA130_head
{
this:
np:hasAssertion
dgn-np:NP876263.RAXTZidu6vxFrvnOrFEHIO4BeWQz52K79U6fj9c-8nbNA130_assertion
;
np:hasProvenance
dgn-np:NP876263.RAXTZidu6vxFrvnOrFEHIO4BeWQz52K79U6fj9c-8nbNA130_provenance
;
np:hasPublicationInfo
dgn-np:NP876263.RAXTZidu6vxFrvnOrFEHIO4BeWQz52K79U6fj9c-8nbNA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP876263.RAXTZidu6vxFrvnOrFEHIO4BeWQz52K79U6fj9c-8nbNA130_assertion
a
np:Assertion
.
dgn-np:NP876263.RAXTZidu6vxFrvnOrFEHIO4BeWQz52K79U6fj9c-8nbNA130_provenance
a
np:Provenance
.
dgn-np:NP876263.RAXTZidu6vxFrvnOrFEHIO4BeWQz52K79U6fj9c-8nbNA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP876263.RAXTZidu6vxFrvnOrFEHIO4BeWQz52K79U6fj9c-8nbNA130_assertion
{
miriam-gene:92304
a
ncit:C16612
.
lld:C1336708
a
ncit:C7057
.
dgn-gda:DGN797aabfe6313b78b841d082e85a47766
sio:SIO_000628
miriam-gene:92304
,
lld:C1336708
;
a
sio:SIO_001121
.
}
dgn-np:NP876263.RAXTZidu6vxFrvnOrFEHIO4BeWQz52K79U6fj9c-8nbNA130_provenance
{
dgn-np:NP876263.RAXTZidu6vxFrvnOrFEHIO4BeWQz52K79U6fj9c-8nbNA130_assertion
dcterms:description
"[In conclusion, this study has identified several novel epigenetically deregulated target genes in TGCT development, including homeobox genes and SCGB3A1, suggesting that epigenetic inactivation of key genes in normal development also has an important role in TGCTs.]. 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:17029216
;
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:NP876263.RAXTZidu6vxFrvnOrFEHIO4BeWQz52K79U6fj9c-8nbNA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:55+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" .
}