@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP204180.RAmz7u1M0w0arEE-xSsLPEUt0-r_SGfEL7xTX7-IC6T34
> .
@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:NP204180.RAmz7u1M0w0arEE-xSsLPEUt0-r_SGfEL7xTX7-IC6T34130_head
{
this:
np:hasAssertion
dgn-np:NP204180.RAmz7u1M0w0arEE-xSsLPEUt0-r_SGfEL7xTX7-IC6T34130_assertion
;
np:hasProvenance
dgn-np:NP204180.RAmz7u1M0w0arEE-xSsLPEUt0-r_SGfEL7xTX7-IC6T34130_provenance
;
np:hasPublicationInfo
dgn-np:NP204180.RAmz7u1M0w0arEE-xSsLPEUt0-r_SGfEL7xTX7-IC6T34130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP204180.RAmz7u1M0w0arEE-xSsLPEUt0-r_SGfEL7xTX7-IC6T34130_assertion
a
np:Assertion
.
dgn-np:NP204180.RAmz7u1M0w0arEE-xSsLPEUt0-r_SGfEL7xTX7-IC6T34130_provenance
a
np:Provenance
.
dgn-np:NP204180.RAmz7u1M0w0arEE-xSsLPEUt0-r_SGfEL7xTX7-IC6T34130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP204180.RAmz7u1M0w0arEE-xSsLPEUt0-r_SGfEL7xTX7-IC6T34130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0206734
a
ncit:C7057
.
dgn-gda:DGNa44cafad89aeb55921e7fe06e1a69636
sio:SIO_000628
miriam-gene:7428
,
lld:C0206734
;
a
sio:SIO_001121
.
}
dgn-np:NP204180.RAmz7u1M0w0arEE-xSsLPEUt0-r_SGfEL7xTX7-IC6T34130_provenance
{
dgn-np:NP204180.RAmz7u1M0w0arEE-xSsLPEUt0-r_SGfEL7xTX7-IC6T34130_assertion
dcterms:description
"[Early detection of VHL disease is important to reduce morbidity and mortality and therefore we recommend that, in addition to conventional clinical and radiological investigations, VHL gene mutation analysis should be offered to all HAB patients younger than 50 years.]. 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:11106358
;
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:NP204180.RAmz7u1M0w0arEE-xSsLPEUt0-r_SGfEL7xTX7-IC6T34130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:52+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" .
}