@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP315809.RAX8SWDKxVJ7Ls4PxTuY5lMYSLdY-0Nvb2djzXr8jg5vg
> .
@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:NP315809.RAX8SWDKxVJ7Ls4PxTuY5lMYSLdY-0Nvb2djzXr8jg5vg130_head
{
this:
np:hasAssertion
dgn-np:NP315809.RAX8SWDKxVJ7Ls4PxTuY5lMYSLdY-0Nvb2djzXr8jg5vg130_assertion
;
np:hasProvenance
dgn-np:NP315809.RAX8SWDKxVJ7Ls4PxTuY5lMYSLdY-0Nvb2djzXr8jg5vg130_provenance
;
np:hasPublicationInfo
dgn-np:NP315809.RAX8SWDKxVJ7Ls4PxTuY5lMYSLdY-0Nvb2djzXr8jg5vg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP315809.RAX8SWDKxVJ7Ls4PxTuY5lMYSLdY-0Nvb2djzXr8jg5vg130_assertion
a
np:Assertion
.
dgn-np:NP315809.RAX8SWDKxVJ7Ls4PxTuY5lMYSLdY-0Nvb2djzXr8jg5vg130_provenance
a
np:Provenance
.
dgn-np:NP315809.RAX8SWDKxVJ7Ls4PxTuY5lMYSLdY-0Nvb2djzXr8jg5vg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP315809.RAX8SWDKxVJ7Ls4PxTuY5lMYSLdY-0Nvb2djzXr8jg5vg130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0022665
a
ncit:C7057
.
dgn-gda:DGNeedd22ac1be2092fc3bf30520c08e081
sio:SIO_000628
miriam-gene:2272
,
lld:C0022665
;
a
sio:SIO_001121
.
}
dgn-np:NP315809.RAX8SWDKxVJ7Ls4PxTuY5lMYSLdY-0Nvb2djzXr8jg5vg130_provenance
{
dgn-np:NP315809.RAX8SWDKxVJ7Ls4PxTuY5lMYSLdY-0Nvb2djzXr8jg5vg130_assertion
dcterms:description
"[To cytogenetically characterize 24 renal tumors in order to check the incidence and the type of 3p deletions, as well as to identify new genes putatively participating in renal tumorigenesis and test the protein products of the von Hippel-Lindau (VHL) and fragile histidine triad (FHIT) genes.]. 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:18517280
;
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:NP315809.RAX8SWDKxVJ7Ls4PxTuY5lMYSLdY-0Nvb2djzXr8jg5vg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:01+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" .
}