@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP432412.RADhFtOWMkSjzfKnMBQjgeT0AMz1jl-oMqbuZcTUsJVfg
> .
@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:NP432412.RADhFtOWMkSjzfKnMBQjgeT0AMz1jl-oMqbuZcTUsJVfg130_head
{
this:
np:hasAssertion
dgn-np:NP432412.RADhFtOWMkSjzfKnMBQjgeT0AMz1jl-oMqbuZcTUsJVfg130_assertion
;
np:hasProvenance
dgn-np:NP432412.RADhFtOWMkSjzfKnMBQjgeT0AMz1jl-oMqbuZcTUsJVfg130_provenance
;
np:hasPublicationInfo
dgn-np:NP432412.RADhFtOWMkSjzfKnMBQjgeT0AMz1jl-oMqbuZcTUsJVfg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP432412.RADhFtOWMkSjzfKnMBQjgeT0AMz1jl-oMqbuZcTUsJVfg130_assertion
a
np:Assertion
.
dgn-np:NP432412.RADhFtOWMkSjzfKnMBQjgeT0AMz1jl-oMqbuZcTUsJVfg130_provenance
a
np:Provenance
.
dgn-np:NP432412.RADhFtOWMkSjzfKnMBQjgeT0AMz1jl-oMqbuZcTUsJVfg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP432412.RADhFtOWMkSjzfKnMBQjgeT0AMz1jl-oMqbuZcTUsJVfg130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0031511
a
ncit:C7057
.
dgn-gda:DGNe879dead94bfbdde81ec4e5fa0aa9034
sio:SIO_000628
miriam-gene:5979
,
lld:C0031511
;
a
sio:SIO_001121
.
}
dgn-np:NP432412.RADhFtOWMkSjzfKnMBQjgeT0AMz1jl-oMqbuZcTUsJVfg130_provenance
{
dgn-np:NP432412.RADhFtOWMkSjzfKnMBQjgeT0AMz1jl-oMqbuZcTUsJVfg130_assertion
dcterms:description
"[Despite the very recent discovery that about 25% of apparently sporadic forms of pheochromocytoma are actually due to germline mutations of RET, VHL, SDHB or SDHD genes, the genetic bases of the tumourigenesis of this type of cancer are still incompletely understood.]. 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:14974911
;
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:NP432412.RADhFtOWMkSjzfKnMBQjgeT0AMz1jl-oMqbuZcTUsJVfg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:01+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" .
}