@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI
> .
@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:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_head
{
this:
np:hasAssertion
dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_assertion
;
np:hasProvenance
dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_provenance
;
np:hasPublicationInfo
dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_assertion
a
np:Assertion
.
dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_provenance
a
np:Provenance
.
dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_assertion
{
miriam-gene:6390
a
ncit:C16612
.
lld:C0031511
a
ncit:C7057
.
dgn-gda:DGN0dccf88c485e11ae3b3ee2b03fcaa788
sio:SIO_000628
miriam-gene:6390
,
lld:C0031511
;
a
sio:SIO_001121
.
}
dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_provenance
{
dgn-np:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_assertion
dcterms:description
"[In the last few years several papers have reported on the association between mutations of the genes encoding the structural (SDHC, SDHD) and catalytic (SDHB) subunits of succinate dehydrogenase and the occurrence of hereditary pheochromocytomas/paragangliomas (Pheo/PGL) syndromes.]. 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:19411806
;
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:NP171721.RA2BWf15_5nazzi1268YJBMn-DUjWM4vTxNhPlPbdfdjI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:32+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" .
}