@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708442.RA7avsd_wPxZkS-nZQY2Z1zzpU7YsKEnM75AQhmkuGD74
> .
@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:NP708442.RA7avsd_wPxZkS-nZQY2Z1zzpU7YsKEnM75AQhmkuGD74130_head
{
this:
np:hasAssertion
dgn-np:NP708442.RA7avsd_wPxZkS-nZQY2Z1zzpU7YsKEnM75AQhmkuGD74130_assertion
;
np:hasProvenance
dgn-np:NP708442.RA7avsd_wPxZkS-nZQY2Z1zzpU7YsKEnM75AQhmkuGD74130_provenance
;
np:hasPublicationInfo
dgn-np:NP708442.RA7avsd_wPxZkS-nZQY2Z1zzpU7YsKEnM75AQhmkuGD74130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708442.RA7avsd_wPxZkS-nZQY2Z1zzpU7YsKEnM75AQhmkuGD74130_assertion
a
np:Assertion
.
dgn-np:NP708442.RA7avsd_wPxZkS-nZQY2Z1zzpU7YsKEnM75AQhmkuGD74130_provenance
a
np:Provenance
.
dgn-np:NP708442.RA7avsd_wPxZkS-nZQY2Z1zzpU7YsKEnM75AQhmkuGD74130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708442.RA7avsd_wPxZkS-nZQY2Z1zzpU7YsKEnM75AQhmkuGD74130_assertion
{
miriam-gene:6392
a
ncit:C16612
.
lld:C0019562
a
ncit:C7057
.
dgn-gda:DGN6c2bc611476e31cf99513ca7959a9d5e
sio:SIO_000628
miriam-gene:6392
,
lld:C0019562
;
a
sio:SIO_001121
.
}
dgn-np:NP708442.RA7avsd_wPxZkS-nZQY2Z1zzpU7YsKEnM75AQhmkuGD74130_provenance
{
dgn-np:NP708442.RA7avsd_wPxZkS-nZQY2Z1zzpU7YsKEnM75AQhmkuGD74130_assertion
dcterms:description
"[Germline VHL mutations may be detected in 5-11% of all phaeochromocytoma cases and mutation analysis of VHL and other phaeochromocytoma susceptibility genes (SDHB, SDHD and RET) should be performed in all cases of familial, multiple or early onset phaeochromocytomas, and considered in other cases.]. 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:16728571
;
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:NP708442.RA7avsd_wPxZkS-nZQY2Z1zzpU7YsKEnM75AQhmkuGD74130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}