@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP430469.RA2g_SeOibqsrDQmK8tUwb3mPcnEfrK-AE0PAh_nT-Z_A
> .
@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:NP430469.RA2g_SeOibqsrDQmK8tUwb3mPcnEfrK-AE0PAh_nT-Z_A130_head
{
this:
np:hasAssertion
dgn-np:NP430469.RA2g_SeOibqsrDQmK8tUwb3mPcnEfrK-AE0PAh_nT-Z_A130_assertion
;
np:hasProvenance
dgn-np:NP430469.RA2g_SeOibqsrDQmK8tUwb3mPcnEfrK-AE0PAh_nT-Z_A130_provenance
;
np:hasPublicationInfo
dgn-np:NP430469.RA2g_SeOibqsrDQmK8tUwb3mPcnEfrK-AE0PAh_nT-Z_A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP430469.RA2g_SeOibqsrDQmK8tUwb3mPcnEfrK-AE0PAh_nT-Z_A130_assertion
a
np:Assertion
.
dgn-np:NP430469.RA2g_SeOibqsrDQmK8tUwb3mPcnEfrK-AE0PAh_nT-Z_A130_provenance
a
np:Provenance
.
dgn-np:NP430469.RA2g_SeOibqsrDQmK8tUwb3mPcnEfrK-AE0PAh_nT-Z_A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP430469.RA2g_SeOibqsrDQmK8tUwb3mPcnEfrK-AE0PAh_nT-Z_A130_assertion
{
miriam-gene:4613
a
ncit:C16612
.
lld:C0025149
a
ncit:C7057
.
dgn-gda:DGNa24237553adc2c38ef20f1e3edde6efb
sio:SIO_000628
miriam-gene:4613
,
lld:C0025149
;
a
sio:SIO_001121
.
}
dgn-np:NP430469.RA2g_SeOibqsrDQmK8tUwb3mPcnEfrK-AE0PAh_nT-Z_A130_provenance
{
dgn-np:NP430469.RA2g_SeOibqsrDQmK8tUwb3mPcnEfrK-AE0PAh_nT-Z_A130_assertion
dcterms:description
"[The amplification of oncogenes seems to play an important role in the pathogenesis of MB, and the association between MYCN and TERT amplifications and poor prognosis has not been well recognized.]. 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:16965953
;
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:NP430469.RA2g_SeOibqsrDQmK8tUwb3mPcnEfrK-AE0PAh_nT-Z_A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+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" .
}