@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP560579.RAESXmAwUnv5SoYh8VFDOvMTOXNOHtgZxWgX_1tfNfCZw
> .
@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:NP560579.RAESXmAwUnv5SoYh8VFDOvMTOXNOHtgZxWgX_1tfNfCZw130_head
{
this:
np:hasAssertion
dgn-np:NP560579.RAESXmAwUnv5SoYh8VFDOvMTOXNOHtgZxWgX_1tfNfCZw130_assertion
;
np:hasProvenance
dgn-np:NP560579.RAESXmAwUnv5SoYh8VFDOvMTOXNOHtgZxWgX_1tfNfCZw130_provenance
;
np:hasPublicationInfo
dgn-np:NP560579.RAESXmAwUnv5SoYh8VFDOvMTOXNOHtgZxWgX_1tfNfCZw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP560579.RAESXmAwUnv5SoYh8VFDOvMTOXNOHtgZxWgX_1tfNfCZw130_assertion
a
np:Assertion
.
dgn-np:NP560579.RAESXmAwUnv5SoYh8VFDOvMTOXNOHtgZxWgX_1tfNfCZw130_provenance
a
np:Provenance
.
dgn-np:NP560579.RAESXmAwUnv5SoYh8VFDOvMTOXNOHtgZxWgX_1tfNfCZw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP560579.RAESXmAwUnv5SoYh8VFDOvMTOXNOHtgZxWgX_1tfNfCZw130_assertion
{
miriam-gene:1630
a
ncit:C16612
.
lld:C0025149
a
ncit:C7057
.
dgn-gda:DGN1f77cb572bfe0358fa82b06db5f1e1ca
sio:SIO_000628
miriam-gene:1630
,
lld:C0025149
;
a
sio:SIO_001121
.
}
dgn-np:NP560579.RAESXmAwUnv5SoYh8VFDOvMTOXNOHtgZxWgX_1tfNfCZw130_provenance
{
dgn-np:NP560579.RAESXmAwUnv5SoYh8VFDOvMTOXNOHtgZxWgX_1tfNfCZw130_assertion
dcterms:description
"[In contrast to the frequent loss of DCC expression, no alterations in NGN expression were observed in more than 50 cancers studied, including glioblastoma, medulloblastoma, neuroblastoma, colorectal, breast, cervical and pancreatic cancer cell lines and xenografts.]. 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:9121761
;
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:NP560579.RAESXmAwUnv5SoYh8VFDOvMTOXNOHtgZxWgX_1tfNfCZw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}