@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1400598.RAqcP-G6XZNI0Dazghjqu93uf_Z8APmGrbvp5ZgJkDN3M
> .
@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:NP1400598.RAqcP-G6XZNI0Dazghjqu93uf_Z8APmGrbvp5ZgJkDN3M130_head
{
this:
np:hasAssertion
dgn-np:NP1400598.RAqcP-G6XZNI0Dazghjqu93uf_Z8APmGrbvp5ZgJkDN3M130_assertion
;
np:hasProvenance
dgn-np:NP1400598.RAqcP-G6XZNI0Dazghjqu93uf_Z8APmGrbvp5ZgJkDN3M130_provenance
;
np:hasPublicationInfo
dgn-np:NP1400598.RAqcP-G6XZNI0Dazghjqu93uf_Z8APmGrbvp5ZgJkDN3M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1400598.RAqcP-G6XZNI0Dazghjqu93uf_Z8APmGrbvp5ZgJkDN3M130_assertion
a
np:Assertion
.
dgn-np:NP1400598.RAqcP-G6XZNI0Dazghjqu93uf_Z8APmGrbvp5ZgJkDN3M130_provenance
a
np:Provenance
.
dgn-np:NP1400598.RAqcP-G6XZNI0Dazghjqu93uf_Z8APmGrbvp5ZgJkDN3M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1400598.RAqcP-G6XZNI0Dazghjqu93uf_Z8APmGrbvp5ZgJkDN3M130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0279702
a
ncit:C7057
.
dgn-gda:DGN83fcd73b2581d841f64d721bf65e394b
sio:SIO_000628
miriam-gene:7428
,
lld:C0279702
;
a
sio:SIO_001121
.
}
dgn-np:NP1400598.RAqcP-G6XZNI0Dazghjqu93uf_Z8APmGrbvp5ZgJkDN3M130_provenance
{
dgn-np:NP1400598.RAqcP-G6XZNI0Dazghjqu93uf_Z8APmGrbvp5ZgJkDN3M130_assertion
dcterms:description
"[Results to date suggest that a substantial proportion of patients with familial pheochromocytoma have VHL gene mutations but in contrast, most familial clusters of clear cell renal cell carcinoma (RCC) without evidence of VHL do not have germline VHL mutations.]. 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:9681854
;
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:NP1400598.RAqcP-G6XZNI0Dazghjqu93uf_Z8APmGrbvp5ZgJkDN3M130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:21+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" .
}