@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP505538.RAq2-Aph0LXulO6A5YY6c2XdDuNySOVur_fXAj89XUYC4
> .
@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:NP505538.RAq2-Aph0LXulO6A5YY6c2XdDuNySOVur_fXAj89XUYC4130_head
{
this:
np:hasAssertion
dgn-np:NP505538.RAq2-Aph0LXulO6A5YY6c2XdDuNySOVur_fXAj89XUYC4130_assertion
;
np:hasProvenance
dgn-np:NP505538.RAq2-Aph0LXulO6A5YY6c2XdDuNySOVur_fXAj89XUYC4130_provenance
;
np:hasPublicationInfo
dgn-np:NP505538.RAq2-Aph0LXulO6A5YY6c2XdDuNySOVur_fXAj89XUYC4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP505538.RAq2-Aph0LXulO6A5YY6c2XdDuNySOVur_fXAj89XUYC4130_assertion
a
np:Assertion
.
dgn-np:NP505538.RAq2-Aph0LXulO6A5YY6c2XdDuNySOVur_fXAj89XUYC4130_provenance
a
np:Provenance
.
dgn-np:NP505538.RAq2-Aph0LXulO6A5YY6c2XdDuNySOVur_fXAj89XUYC4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP505538.RAq2-Aph0LXulO6A5YY6c2XdDuNySOVur_fXAj89XUYC4130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0031511
a
ncit:C7057
.
dgn-gda:DGN1d91513657acacf6216d3e3a7dc5b4df
sio:SIO_000628
miriam-gene:7428
,
lld:C0031511
;
a
sio:SIO_001121
.
}
dgn-np:NP505538.RAq2-Aph0LXulO6A5YY6c2XdDuNySOVur_fXAj89XUYC4130_provenance
{
dgn-np:NP505538.RAq2-Aph0LXulO6A5YY6c2XdDuNySOVur_fXAj89XUYC4130_assertion
dcterms:description
"[The frequency of de novo mutations in susceptible genes (especially the VHL gene) in paediatric patients with sporadic phaeochromocytoma and the elevated mortality of these cancer syndromes suggest that screening for mutations should be performed even in cases of non-familial sporadic phaeochromocytoma.]. 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:16042317
;
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:NP505538.RAq2-Aph0LXulO6A5YY6c2XdDuNySOVur_fXAj89XUYC4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:34+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" .
}