@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1278581.RAVdWvVikxI6Pm-gMD-StTHRXQ0DJ0WeV7XGB9psVkO6c
> .
@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:NP1278581.RAVdWvVikxI6Pm-gMD-StTHRXQ0DJ0WeV7XGB9psVkO6c130_head
{
this:
np:hasAssertion
dgn-np:NP1278581.RAVdWvVikxI6Pm-gMD-StTHRXQ0DJ0WeV7XGB9psVkO6c130_assertion
;
np:hasProvenance
dgn-np:NP1278581.RAVdWvVikxI6Pm-gMD-StTHRXQ0DJ0WeV7XGB9psVkO6c130_provenance
;
np:hasPublicationInfo
dgn-np:NP1278581.RAVdWvVikxI6Pm-gMD-StTHRXQ0DJ0WeV7XGB9psVkO6c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1278581.RAVdWvVikxI6Pm-gMD-StTHRXQ0DJ0WeV7XGB9psVkO6c130_assertion
a
np:Assertion
.
dgn-np:NP1278581.RAVdWvVikxI6Pm-gMD-StTHRXQ0DJ0WeV7XGB9psVkO6c130_provenance
a
np:Provenance
.
dgn-np:NP1278581.RAVdWvVikxI6Pm-gMD-StTHRXQ0DJ0WeV7XGB9psVkO6c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1278581.RAVdWvVikxI6Pm-gMD-StTHRXQ0DJ0WeV7XGB9psVkO6c130_assertion
{
miriam-gene:238
a
ncit:C16612
.
lld:C0027819
a
ncit:C7057
.
dgn-gda:DGNd39f76f2e4893eba1756553bd962a3c8
sio:SIO_000628
miriam-gene:238
,
lld:C0027819
;
a
sio:SIO_001121
.
}
dgn-np:NP1278581.RAVdWvVikxI6Pm-gMD-StTHRXQ0DJ0WeV7XGB9psVkO6c130_provenance
{
dgn-np:NP1278581.RAVdWvVikxI6Pm-gMD-StTHRXQ0DJ0WeV7XGB9psVkO6c130_assertion
dcterms:description
"[The pathogenetic role of PHOX2B in neuroblastoma (NB) is supported by mutations in familial, sporadic and syndromic cases of NB and overexpression of PHOX2B and its target ALK in tumor samples and NB cell lines.]. 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:25882494
;
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:NP1278581.RAVdWvVikxI6Pm-gMD-StTHRXQ0DJ0WeV7XGB9psVkO6c130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:25+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" .
}