@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw
> .
@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:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_head
{
this:
np:hasAssertion
dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_assertion
;
np:hasProvenance
dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_provenance
;
np:hasPublicationInfo
dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_assertion
a
np:Assertion
.
dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_provenance
a
np:Provenance
.
dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0019562
a
ncit:C7057
.
dgn-gda:DGNc78462e6764d8fdfdc41fcb0581d49dd
sio:SIO_000628
miriam-gene:7428
,
lld:C0019562
;
a
sio:SIO_001121
.
}
dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_provenance
{
dgn-np:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_assertion
dcterms:description
"[von Hippel-Lindau (VHL) disease is an autosomal dominant inherited tumor syndrome characterized by the development of tumors in the eye, brain, spinal cord, inner ear, adrenal gland, pancreas, kidney, and epididymis, associated with germline mutations in the VHL gene.]. 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:19270817
;
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:NP724664.RArF_5mrWJV2SQlD-rmNIZhGiK4c7U2nuzrfucj9vqNBw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:13+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" .
}