@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP709313.RAiMiaCAHsWvHcWQP3upx6XzwpXOgi8DTzDAEHC2FnGvw
> .
@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:NP709313.RAiMiaCAHsWvHcWQP3upx6XzwpXOgi8DTzDAEHC2FnGvw130_head
{
this:
np:hasAssertion
dgn-np:NP709313.RAiMiaCAHsWvHcWQP3upx6XzwpXOgi8DTzDAEHC2FnGvw130_assertion
;
np:hasProvenance
dgn-np:NP709313.RAiMiaCAHsWvHcWQP3upx6XzwpXOgi8DTzDAEHC2FnGvw130_provenance
;
np:hasPublicationInfo
dgn-np:NP709313.RAiMiaCAHsWvHcWQP3upx6XzwpXOgi8DTzDAEHC2FnGvw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP709313.RAiMiaCAHsWvHcWQP3upx6XzwpXOgi8DTzDAEHC2FnGvw130_assertion
a
np:Assertion
.
dgn-np:NP709313.RAiMiaCAHsWvHcWQP3upx6XzwpXOgi8DTzDAEHC2FnGvw130_provenance
a
np:Provenance
.
dgn-np:NP709313.RAiMiaCAHsWvHcWQP3upx6XzwpXOgi8DTzDAEHC2FnGvw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP709313.RAiMiaCAHsWvHcWQP3upx6XzwpXOgi8DTzDAEHC2FnGvw130_assertion
{
miriam-gene:8929
a
ncit:C16612
.
lld:C0031511
a
ncit:C7057
.
dgn-gda:DGNd6e56d46ef4cdd7d9cd87b5fb511018c
sio:SIO_000628
miriam-gene:8929
,
lld:C0031511
;
a
sio:SIO_001121
.
}
dgn-np:NP709313.RAiMiaCAHsWvHcWQP3upx6XzwpXOgi8DTzDAEHC2FnGvw130_provenance
{
dgn-np:NP709313.RAiMiaCAHsWvHcWQP3upx6XzwpXOgi8DTzDAEHC2FnGvw130_assertion
dcterms:description
"[We observed PHOX2B expression in all peripheral neuroblastic tumors, paragangliomas, and pheochromocytomas tested but in no other pediatric tumors among the 388 cases studied by expression microarray and the 109 cases studied by immunohistochemical analysis.]. 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:22790854
;
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:NP709313.RAiMiaCAHsWvHcWQP3upx6XzwpXOgi8DTzDAEHC2FnGvw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:11+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" .
}