@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8
> .
@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:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_head
{
this:
np:hasAssertion
dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_assertion
;
np:hasProvenance
dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance
;
np:hasPublicationInfo
dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_assertion
a
np:Assertion
.
dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance
a
np:Provenance
.
dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_assertion
{
miriam-gene:113675
a
ncit:C16612
.
lld:C0030421
a
ncit:C7057
.
dgn-gda:DGN01e4c24717b9701467bce6ad376d7fa1
sio:SIO_000628
miriam-gene:113675
,
lld:C0030421
;
a
sio:SIO_001121
.
}
dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_provenance
{
dgn-np:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_assertion
dcterms:description
"[Approximately 10% to 15% of paragangliomas are caused by mutations in the succinate dehydrogenase (SDH) genes B, C, or D. These are often multifocal as part of paraganglioma syndromes and hormone secreting, and malignant particularly associated with mutations in SDHB.]. 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:18213727
;
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:NP202153.RAEp17WSyAROQDll_zfkUVUT7ZS-F5DGA6N4XzicTATt8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:51+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" .
}