@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII
> .
@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#
> .
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{
this:
np:hasAssertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_assertion
a
np:Assertion
.
dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_provenance
a
np:Provenance
.
dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_publicationInfo
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np:PublicationInfo
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dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_assertion
{
miriam-gene:6390
a
ncit:C16612
.
lld:C1333993
a
ncit:C7057
.
dgn-gda:DGN3a0b8efc11df2837ddc0cd21ac3745af
sio:SIO_000628
miriam-gene:6390
,
lld:C1333993
;
a
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.
}
dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_provenance
{
dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_assertion
dcterms:description
"[A question confronting clinicians is whether they should screen patients with apparently sporadic pheochromocytomas for unsuspected germline mutations of some or all of the seven genes known to cause hereditary paraganglioma or pheochromocytoma (NF1, VHL, RET, MEN1, SDHD, SDHC, and 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:16735498
;
prov:wasDerivedFrom
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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 .
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dgn-np:NP161348.RADbKDVkprP6jeylChNhFuGg2UwnUDn68ZaoiJ-VJtaII130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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
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> , <
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> , <
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> ;
pav:createdBy
<
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