@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP199773.RAyN15cKwZBX_eLRamb8v1cND6QhTZ3O0lFSiTPalHW3Q
> .
@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:NP199773.RAyN15cKwZBX_eLRamb8v1cND6QhTZ3O0lFSiTPalHW3Q130_head
{
this:
np:hasAssertion
dgn-np:NP199773.RAyN15cKwZBX_eLRamb8v1cND6QhTZ3O0lFSiTPalHW3Q130_assertion
;
np:hasProvenance
dgn-np:NP199773.RAyN15cKwZBX_eLRamb8v1cND6QhTZ3O0lFSiTPalHW3Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP199773.RAyN15cKwZBX_eLRamb8v1cND6QhTZ3O0lFSiTPalHW3Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP199773.RAyN15cKwZBX_eLRamb8v1cND6QhTZ3O0lFSiTPalHW3Q130_assertion
a
np:Assertion
.
dgn-np:NP199773.RAyN15cKwZBX_eLRamb8v1cND6QhTZ3O0lFSiTPalHW3Q130_provenance
a
np:Provenance
.
dgn-np:NP199773.RAyN15cKwZBX_eLRamb8v1cND6QhTZ3O0lFSiTPalHW3Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP199773.RAyN15cKwZBX_eLRamb8v1cND6QhTZ3O0lFSiTPalHW3Q130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0031511
a
ncit:C7057
.
dgn-gda:DGN8ef69ccdc94991a7cbd6eb6656ba0ad4
sio:SIO_000628
miriam-gene:4221
,
lld:C0031511
;
a
sio:SIO_001121
.
}
dgn-np:NP199773.RAyN15cKwZBX_eLRamb8v1cND6QhTZ3O0lFSiTPalHW3Q130_provenance
{
dgn-np:NP199773.RAyN15cKwZBX_eLRamb8v1cND6QhTZ3O0lFSiTPalHW3Q130_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
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:NP199773.RAyN15cKwZBX_eLRamb8v1cND6QhTZ3O0lFSiTPalHW3Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:50+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" .
}