@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP170187.RAuRn7nBxN_7yCnWK21raUmDD7EfzUBnVl-8sNp7X_QDM
> .
@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:NP170187.RAuRn7nBxN_7yCnWK21raUmDD7EfzUBnVl-8sNp7X_QDM130_head
{
this:
np:hasAssertion
dgn-np:NP170187.RAuRn7nBxN_7yCnWK21raUmDD7EfzUBnVl-8sNp7X_QDM130_assertion
;
np:hasProvenance
dgn-np:NP170187.RAuRn7nBxN_7yCnWK21raUmDD7EfzUBnVl-8sNp7X_QDM130_provenance
;
np:hasPublicationInfo
dgn-np:NP170187.RAuRn7nBxN_7yCnWK21raUmDD7EfzUBnVl-8sNp7X_QDM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP170187.RAuRn7nBxN_7yCnWK21raUmDD7EfzUBnVl-8sNp7X_QDM130_assertion
a
np:Assertion
.
dgn-np:NP170187.RAuRn7nBxN_7yCnWK21raUmDD7EfzUBnVl-8sNp7X_QDM130_provenance
a
np:Provenance
.
dgn-np:NP170187.RAuRn7nBxN_7yCnWK21raUmDD7EfzUBnVl-8sNp7X_QDM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP170187.RAuRn7nBxN_7yCnWK21raUmDD7EfzUBnVl-8sNp7X_QDM130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0019562
a
ncit:C7057
.
dgn-gda:DGN7292e76bbe6ed67490ddc1304f598efe
sio:SIO_000628
miriam-gene:7428
,
lld:C0019562
;
a
sio:SIO_001121
.
}
dgn-np:NP170187.RAuRn7nBxN_7yCnWK21raUmDD7EfzUBnVl-8sNp7X_QDM130_provenance
{
dgn-np:NP170187.RAuRn7nBxN_7yCnWK21raUmDD7EfzUBnVl-8sNp7X_QDM130_assertion
dcterms:description
"[To investigate the genetic profile of VHL mutations in the Chinese population, we evaluated the clinical characteristics of seven Chinese families suffering from VHL disease and determined the particular germline mutations in their VHL 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:21972040
;
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:NP170187.RAuRn7nBxN_7yCnWK21raUmDD7EfzUBnVl-8sNp7X_QDM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:32+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" .
}