@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP509300.RAH52Z_6DxUhb-39o-PoydqFNUPtF7CF-EQ91-wgZYwx4
> .
@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:NP509300.RAH52Z_6DxUhb-39o-PoydqFNUPtF7CF-EQ91-wgZYwx4130_head
{
this:
np:hasAssertion
dgn-np:NP509300.RAH52Z_6DxUhb-39o-PoydqFNUPtF7CF-EQ91-wgZYwx4130_assertion
;
np:hasProvenance
dgn-np:NP509300.RAH52Z_6DxUhb-39o-PoydqFNUPtF7CF-EQ91-wgZYwx4130_provenance
;
np:hasPublicationInfo
dgn-np:NP509300.RAH52Z_6DxUhb-39o-PoydqFNUPtF7CF-EQ91-wgZYwx4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP509300.RAH52Z_6DxUhb-39o-PoydqFNUPtF7CF-EQ91-wgZYwx4130_assertion
a
np:Assertion
.
dgn-np:NP509300.RAH52Z_6DxUhb-39o-PoydqFNUPtF7CF-EQ91-wgZYwx4130_provenance
a
np:Provenance
.
dgn-np:NP509300.RAH52Z_6DxUhb-39o-PoydqFNUPtF7CF-EQ91-wgZYwx4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP509300.RAH52Z_6DxUhb-39o-PoydqFNUPtF7CF-EQ91-wgZYwx4130_assertion
{
miriam-gene:2026
a
ncit:C16612
.
lld:C0027819
a
ncit:C7057
.
dgn-gda:DGN31abe5a5a660d672a8d1d4b71968b02e
sio:SIO_000628
miriam-gene:2026
,
lld:C0027819
;
a
sio:SIO_001121
.
}
dgn-np:NP509300.RAH52Z_6DxUhb-39o-PoydqFNUPtF7CF-EQ91-wgZYwx4130_provenance
{
dgn-np:NP509300.RAH52Z_6DxUhb-39o-PoydqFNUPtF7CF-EQ91-wgZYwx4130_assertion
dcterms:description
"[The primary site (adrenal gland) with radiologic findings (with foci of calcification), high titer of serum neuron specific enolase, and sheets of monotonous primitive rounded cells on histology mostly favored neuroblastoma.]. 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:11567233
;
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:NP509300.RAH52Z_6DxUhb-39o-PoydqFNUPtF7CF-EQ91-wgZYwx4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:03+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" .
}