@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1107349.RAO3g0Xnfce9MZUl0pgLVqFxf538doUFQ_-TuCt4IbI3Q
> .
@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:NP1107349.RAO3g0Xnfce9MZUl0pgLVqFxf538doUFQ_-TuCt4IbI3Q130_head
{
this:
np:hasAssertion
dgn-np:NP1107349.RAO3g0Xnfce9MZUl0pgLVqFxf538doUFQ_-TuCt4IbI3Q130_assertion
;
np:hasProvenance
dgn-np:NP1107349.RAO3g0Xnfce9MZUl0pgLVqFxf538doUFQ_-TuCt4IbI3Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP1107349.RAO3g0Xnfce9MZUl0pgLVqFxf538doUFQ_-TuCt4IbI3Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1107349.RAO3g0Xnfce9MZUl0pgLVqFxf538doUFQ_-TuCt4IbI3Q130_assertion
a
np:Assertion
.
dgn-np:NP1107349.RAO3g0Xnfce9MZUl0pgLVqFxf538doUFQ_-TuCt4IbI3Q130_provenance
a
np:Provenance
.
dgn-np:NP1107349.RAO3g0Xnfce9MZUl0pgLVqFxf538doUFQ_-TuCt4IbI3Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1107349.RAO3g0Xnfce9MZUl0pgLVqFxf538doUFQ_-TuCt4IbI3Q130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0007134
a
ncit:C7057
.
dgn-gda:DGNfe060b39c5aec63d4953fcf8927c33c8
sio:SIO_000628
miriam-gene:7428
,
lld:C0007134
;
a
sio:SIO_001121
.
}
dgn-np:NP1107349.RAO3g0Xnfce9MZUl0pgLVqFxf538doUFQ_-TuCt4IbI3Q130_provenance
{
dgn-np:NP1107349.RAO3g0Xnfce9MZUl0pgLVqFxf538doUFQ_-TuCt4IbI3Q130_assertion
dcterms:description
"[Investigation of rare familial forms of renal cell carcinoma (RCC) has led to the identification of genes such as VHL and MET that are also implicated in the pathogenesis of sporadic RCC.]. 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:24000165
;
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:NP1107349.RAO3g0Xnfce9MZUl0pgLVqFxf538doUFQ_-TuCt4IbI3Q130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:08+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" .
}