@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP308497.RAZ-OEc2V_3NVPSimVzu19MwA_lMkVRY0TJEKVGmBKMEI
> .
@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:NP308497.RAZ-OEc2V_3NVPSimVzu19MwA_lMkVRY0TJEKVGmBKMEI130_head
{
this:
np:hasAssertion
dgn-np:NP308497.RAZ-OEc2V_3NVPSimVzu19MwA_lMkVRY0TJEKVGmBKMEI130_assertion
;
np:hasProvenance
dgn-np:NP308497.RAZ-OEc2V_3NVPSimVzu19MwA_lMkVRY0TJEKVGmBKMEI130_provenance
;
np:hasPublicationInfo
dgn-np:NP308497.RAZ-OEc2V_3NVPSimVzu19MwA_lMkVRY0TJEKVGmBKMEI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP308497.RAZ-OEc2V_3NVPSimVzu19MwA_lMkVRY0TJEKVGmBKMEI130_assertion
a
np:Assertion
.
dgn-np:NP308497.RAZ-OEc2V_3NVPSimVzu19MwA_lMkVRY0TJEKVGmBKMEI130_provenance
a
np:Provenance
.
dgn-np:NP308497.RAZ-OEc2V_3NVPSimVzu19MwA_lMkVRY0TJEKVGmBKMEI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP308497.RAZ-OEc2V_3NVPSimVzu19MwA_lMkVRY0TJEKVGmBKMEI130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0740457
a
ncit:C7057
.
dgn-gda:DGN6527048386f3d0bcea898051cc292bfd
sio:SIO_000628
miriam-gene:7428
,
lld:C0740457
;
a
sio:SIO_001121
.
}
dgn-np:NP308497.RAZ-OEc2V_3NVPSimVzu19MwA_lMkVRY0TJEKVGmBKMEI130_provenance
{
dgn-np:NP308497.RAZ-OEc2V_3NVPSimVzu19MwA_lMkVRY0TJEKVGmBKMEI130_assertion
dcterms:description
"[Renal or kidney cancer accounts for about 3% of all cancer cases reported each year in the U.S. Molecular signatures that define the cancer, such as the loss of functional VHL, are found in both sporadic and familial cases of cancer.]. 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:22928967
;
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:NP308497.RAZ-OEc2V_3NVPSimVzu19MwA_lMkVRY0TJEKVGmBKMEI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:57+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" .
}