@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP894445.RAdSWVBsj0mf6xHuw7kpC2XK3xH4JGZURgUfWvxT01pvc
> .
@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:NP894445.RAdSWVBsj0mf6xHuw7kpC2XK3xH4JGZURgUfWvxT01pvc130_head
{
this:
np:hasAssertion
dgn-np:NP894445.RAdSWVBsj0mf6xHuw7kpC2XK3xH4JGZURgUfWvxT01pvc130_assertion
;
np:hasProvenance
dgn-np:NP894445.RAdSWVBsj0mf6xHuw7kpC2XK3xH4JGZURgUfWvxT01pvc130_provenance
;
np:hasPublicationInfo
dgn-np:NP894445.RAdSWVBsj0mf6xHuw7kpC2XK3xH4JGZURgUfWvxT01pvc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP894445.RAdSWVBsj0mf6xHuw7kpC2XK3xH4JGZURgUfWvxT01pvc130_assertion
a
np:Assertion
.
dgn-np:NP894445.RAdSWVBsj0mf6xHuw7kpC2XK3xH4JGZURgUfWvxT01pvc130_provenance
a
np:Provenance
.
dgn-np:NP894445.RAdSWVBsj0mf6xHuw7kpC2XK3xH4JGZURgUfWvxT01pvc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP894445.RAdSWVBsj0mf6xHuw7kpC2XK3xH4JGZURgUfWvxT01pvc130_assertion
{
miriam-gene:25797
a
ncit:C16612
.
lld:C0036875
a
ncit:C7057
.
dgn-gda:DGN6bd870b40795fe207807cfbead1caa72
sio:SIO_000628
miriam-gene:25797
,
lld:C0036875
;
a
sio:SIO_001121
.
}
dgn-np:NP894445.RAdSWVBsj0mf6xHuw7kpC2XK3xH4JGZURgUfWvxT01pvc130_provenance
{
dgn-np:NP894445.RAdSWVBsj0mf6xHuw7kpC2XK3xH4JGZURgUfWvxT01pvc130_assertion
dcterms:description
"[Parallels between the origin of mOGCT and their male counterpart testicular GCT (TGCT) are discussed from the perspective of germ cell development, endocrinological influences, and pathogenesis, as is the GCT origin in patients with disorders of sex development.]. 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:23575763
;
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:NP894445.RAdSWVBsj0mf6xHuw7kpC2XK3xH4JGZURgUfWvxT01pvc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:09+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" .
}