@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP321575.RAuYnkwE0kH4V_K7HXlW2HgQTqRyxEZ24CXUCsE0bjTnI
> .
@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:NP321575.RAuYnkwE0kH4V_K7HXlW2HgQTqRyxEZ24CXUCsE0bjTnI130_head
{
this:
np:hasAssertion
dgn-np:NP321575.RAuYnkwE0kH4V_K7HXlW2HgQTqRyxEZ24CXUCsE0bjTnI130_assertion
;
np:hasProvenance
dgn-np:NP321575.RAuYnkwE0kH4V_K7HXlW2HgQTqRyxEZ24CXUCsE0bjTnI130_provenance
;
np:hasPublicationInfo
dgn-np:NP321575.RAuYnkwE0kH4V_K7HXlW2HgQTqRyxEZ24CXUCsE0bjTnI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP321575.RAuYnkwE0kH4V_K7HXlW2HgQTqRyxEZ24CXUCsE0bjTnI130_assertion
a
np:Assertion
.
dgn-np:NP321575.RAuYnkwE0kH4V_K7HXlW2HgQTqRyxEZ24CXUCsE0bjTnI130_provenance
a
np:Provenance
.
dgn-np:NP321575.RAuYnkwE0kH4V_K7HXlW2HgQTqRyxEZ24CXUCsE0bjTnI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP321575.RAuYnkwE0kH4V_K7HXlW2HgQTqRyxEZ24CXUCsE0bjTnI130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0027831
a
ncit:C7057
.
dgn-gda:DGN7463de95b9d2c8f7848b6f5e7efd4ec3
sio:SIO_000628
miriam-gene:7428
,
lld:C0027831
;
a
sio:SIO_001121
.
}
dgn-np:NP321575.RAuYnkwE0kH4V_K7HXlW2HgQTqRyxEZ24CXUCsE0bjTnI130_provenance
{
dgn-np:NP321575.RAuYnkwE0kH4V_K7HXlW2HgQTqRyxEZ24CXUCsE0bjTnI130_assertion
dcterms:description
"[In the absence of germline mutations in VHL, RET, SDHD, and SDHB, patients with pheochromocytoma, especially with bilateral disease, should be checked thoroughly for clinical lesions suggestive of underlying syndromes such as the cutaneous and ophthalmological features characteristic of NF 1.]. 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:16787982
;
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:NP321575.RAuYnkwE0kH4V_K7HXlW2HgQTqRyxEZ24CXUCsE0bjTnI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:06+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" .
}