@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE
> .
@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:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_head
{
this:
np:hasAssertion
dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_assertion
;
np:hasProvenance
dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_provenance
;
np:hasPublicationInfo
dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_assertion
a
np:Assertion
.
dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_provenance
a
np:Provenance
.
dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_assertion
{
miriam-gene:4613
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN3d7691f2a4ab159069e290ba2a7da476
sio:SIO_000628
miriam-gene:4613
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_provenance
{
dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_assertion
dcterms:description
"[Loss of heterozygosity of the distal region of chromosome 1p where tumor suppressor gene(s) might harbor is frequently observed in many human cancers including neuroblastoma (NBL) with MYCN amplification and poor prognosis.]. 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:10980605
;
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:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:32+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" .
}