@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP369274.RAODCqqfnc_pCqVg1rZsc7aXRfF-A7jBivhdKSfdp4d0k
> .
@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:NP369274.RAODCqqfnc_pCqVg1rZsc7aXRfF-A7jBivhdKSfdp4d0k130_head
{
this:
np:hasAssertion
dgn-np:NP369274.RAODCqqfnc_pCqVg1rZsc7aXRfF-A7jBivhdKSfdp4d0k130_assertion
;
np:hasProvenance
dgn-np:NP369274.RAODCqqfnc_pCqVg1rZsc7aXRfF-A7jBivhdKSfdp4d0k130_provenance
;
np:hasPublicationInfo
dgn-np:NP369274.RAODCqqfnc_pCqVg1rZsc7aXRfF-A7jBivhdKSfdp4d0k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP369274.RAODCqqfnc_pCqVg1rZsc7aXRfF-A7jBivhdKSfdp4d0k130_assertion
a
np:Assertion
.
dgn-np:NP369274.RAODCqqfnc_pCqVg1rZsc7aXRfF-A7jBivhdKSfdp4d0k130_provenance
a
np:Provenance
.
dgn-np:NP369274.RAODCqqfnc_pCqVg1rZsc7aXRfF-A7jBivhdKSfdp4d0k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP369274.RAODCqqfnc_pCqVg1rZsc7aXRfF-A7jBivhdKSfdp4d0k130_assertion
{
miriam-gene:338386
a
ncit:C16612
.
lld:C0700095
a
ncit:C7057
.
dgn-gda:DGNed63096047202793609e374dfde1dd0a
sio:SIO_000628
miriam-gene:338386
,
lld:C0700095
;
a
sio:SIO_001121
.
}
dgn-np:NP369274.RAODCqqfnc_pCqVg1rZsc7aXRfF-A7jBivhdKSfdp4d0k130_provenance
{
dgn-np:NP369274.RAODCqqfnc_pCqVg1rZsc7aXRfF-A7jBivhdKSfdp4d0k130_assertion
dcterms:description
"[MYCN amplification in neuroblastoma tumor cells is manifested primarily as double minutes (dmins), whereas in cell lines it often appears in the form of homogeneously staining regions (HSR), suggesting that HSRs are associated with a more aggressive tumor phenotype and worse clinical outcome.]. 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:17020972
;
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:NP369274.RAODCqqfnc_pCqVg1rZsc7aXRfF-A7jBivhdKSfdp4d0k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:36+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" .
}