@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP240128.RAuFkpDYKCSV7cu-GRbm4GxO6bYuXG3cX3sYp35xSN34w
> .
@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:NP240128.RAuFkpDYKCSV7cu-GRbm4GxO6bYuXG3cX3sYp35xSN34w130_head
{
this:
np:hasAssertion
dgn-np:NP240128.RAuFkpDYKCSV7cu-GRbm4GxO6bYuXG3cX3sYp35xSN34w130_assertion
;
np:hasProvenance
dgn-np:NP240128.RAuFkpDYKCSV7cu-GRbm4GxO6bYuXG3cX3sYp35xSN34w130_provenance
;
np:hasPublicationInfo
dgn-np:NP240128.RAuFkpDYKCSV7cu-GRbm4GxO6bYuXG3cX3sYp35xSN34w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP240128.RAuFkpDYKCSV7cu-GRbm4GxO6bYuXG3cX3sYp35xSN34w130_assertion
a
np:Assertion
.
dgn-np:NP240128.RAuFkpDYKCSV7cu-GRbm4GxO6bYuXG3cX3sYp35xSN34w130_provenance
a
np:Provenance
.
dgn-np:NP240128.RAuFkpDYKCSV7cu-GRbm4GxO6bYuXG3cX3sYp35xSN34w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP240128.RAuFkpDYKCSV7cu-GRbm4GxO6bYuXG3cX3sYp35xSN34w130_assertion
{
miriam-gene:4609
a
ncit:C16612
.
lld:C0205833
a
ncit:C7057
.
dgn-gda:DGNea809fd5164cf0bed498f6ea6806e471
sio:SIO_000628
miriam-gene:4609
,
lld:C0205833
;
a
sio:SIO_001121
.
}
dgn-np:NP240128.RAuFkpDYKCSV7cu-GRbm4GxO6bYuXG3cX3sYp35xSN34w130_provenance
{
dgn-np:NP240128.RAuFkpDYKCSV7cu-GRbm4GxO6bYuXG3cX3sYp35xSN34w130_assertion
dcterms:description
"[Similar to the scenario in classical medulloblastoma, which contains the primitive neuroectodermal component only, gain of sequences from the long arm of chromosome 17 (17q) and gain of the MYC gene in 8q have been implicated in the pathogenesis of MMB.]. 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:18021376
;
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:NP240128.RAuFkpDYKCSV7cu-GRbm4GxO6bYuXG3cX3sYp35xSN34w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}