@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP374417.RAKxurT9mOXR4sjrjfnpZncoCCqg9mGqsGmhYqC8lha1Y
> .
@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:NP374417.RAKxurT9mOXR4sjrjfnpZncoCCqg9mGqsGmhYqC8lha1Y130_head
{
this:
np:hasAssertion
dgn-np:NP374417.RAKxurT9mOXR4sjrjfnpZncoCCqg9mGqsGmhYqC8lha1Y130_assertion
;
np:hasProvenance
dgn-np:NP374417.RAKxurT9mOXR4sjrjfnpZncoCCqg9mGqsGmhYqC8lha1Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP374417.RAKxurT9mOXR4sjrjfnpZncoCCqg9mGqsGmhYqC8lha1Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP374417.RAKxurT9mOXR4sjrjfnpZncoCCqg9mGqsGmhYqC8lha1Y130_assertion
a
np:Assertion
.
dgn-np:NP374417.RAKxurT9mOXR4sjrjfnpZncoCCqg9mGqsGmhYqC8lha1Y130_provenance
a
np:Provenance
.
dgn-np:NP374417.RAKxurT9mOXR4sjrjfnpZncoCCqg9mGqsGmhYqC8lha1Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP374417.RAKxurT9mOXR4sjrjfnpZncoCCqg9mGqsGmhYqC8lha1Y130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C1378703
a
ncit:C7057
.
dgn-gda:DGN51e38809843da2c4fec64a545b4b81b8
sio:SIO_000628
miriam-gene:7428
,
lld:C1378703
;
a
sio:SIO_001121
.
}
dgn-np:NP374417.RAKxurT9mOXR4sjrjfnpZncoCCqg9mGqsGmhYqC8lha1Y130_provenance
{
dgn-np:NP374417.RAKxurT9mOXR4sjrjfnpZncoCCqg9mGqsGmhYqC8lha1Y130_assertion
dcterms:description
"[The aim of this study was to provide a comprehensive analysis of VHL inactivation in clear cell renal tumors (ccRCC) and to evaluate relationships between VHL inactivation subgroups with renal cancer risk factors and VHL germline single nucleotide polymorphisms (SNPs).]. 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:22022277
;
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:NP374417.RAKxurT9mOXR4sjrjfnpZncoCCqg9mGqsGmhYqC8lha1Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:39+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" .
}