@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP294612.RAAVA4f6RYTAjaSbN281B2zRwErsmg9qJBzhB4qUH7nhg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP294612.RAAVA4f6RYTAjaSbN281B2zRwErsmg9qJBzhB4qUH7nhg130_head
{
this:
np:hasAssertion
dgn-np:NP294612.RAAVA4f6RYTAjaSbN281B2zRwErsmg9qJBzhB4qUH7nhg130_assertion
;
np:hasProvenance
dgn-np:NP294612.RAAVA4f6RYTAjaSbN281B2zRwErsmg9qJBzhB4qUH7nhg130_provenance
;
np:hasPublicationInfo
dgn-np:NP294612.RAAVA4f6RYTAjaSbN281B2zRwErsmg9qJBzhB4qUH7nhg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP294612.RAAVA4f6RYTAjaSbN281B2zRwErsmg9qJBzhB4qUH7nhg130_assertion
a
np:Assertion
.
dgn-np:NP294612.RAAVA4f6RYTAjaSbN281B2zRwErsmg9qJBzhB4qUH7nhg130_provenance
a
np:Provenance
.
dgn-np:NP294612.RAAVA4f6RYTAjaSbN281B2zRwErsmg9qJBzhB4qUH7nhg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP294612.RAAVA4f6RYTAjaSbN281B2zRwErsmg9qJBzhB4qUH7nhg130_assertion
{
miriam-gene:4613
a
ncit:C16612
.
lld:C0027819
a
ncit:C7057
.
dgn-gda:DGN7c722ec64caeadd8a6438c9f0c1ce101
sio:SIO_000628
miriam-gene:4613
,
lld:C0027819
;
a
sio:SIO_001121
.
}
dgn-np:NP294612.RAAVA4f6RYTAjaSbN281B2zRwErsmg9qJBzhB4qUH7nhg130_provenance
{
dgn-np:NP294612.RAAVA4f6RYTAjaSbN281B2zRwErsmg9qJBzhB4qUH7nhg130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP294612.RAAVA4f6RYTAjaSbN281B2zRwErsmg9qJBzhB4qUH7nhg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:59+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}