@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP151762.RAUHSCr6UmAR85qrWeoe2rDO1DFYzmAf3oxuB3FJbvTU0
> .
@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:NP151762.RAUHSCr6UmAR85qrWeoe2rDO1DFYzmAf3oxuB3FJbvTU0130_head
{
this:
np:hasAssertion
dgn-np:NP151762.RAUHSCr6UmAR85qrWeoe2rDO1DFYzmAf3oxuB3FJbvTU0130_assertion
;
np:hasProvenance
dgn-np:NP151762.RAUHSCr6UmAR85qrWeoe2rDO1DFYzmAf3oxuB3FJbvTU0130_provenance
;
np:hasPublicationInfo
dgn-np:NP151762.RAUHSCr6UmAR85qrWeoe2rDO1DFYzmAf3oxuB3FJbvTU0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP151762.RAUHSCr6UmAR85qrWeoe2rDO1DFYzmAf3oxuB3FJbvTU0130_assertion
a
np:Assertion
.
dgn-np:NP151762.RAUHSCr6UmAR85qrWeoe2rDO1DFYzmAf3oxuB3FJbvTU0130_provenance
a
np:Provenance
.
dgn-np:NP151762.RAUHSCr6UmAR85qrWeoe2rDO1DFYzmAf3oxuB3FJbvTU0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP151762.RAUHSCr6UmAR85qrWeoe2rDO1DFYzmAf3oxuB3FJbvTU0130_assertion
{
miriam-gene:2271
a
ncit:C16612
.
lld:C0023269
a
ncit:C7057
.
dgn-gda:DGN9c0df135fe13414681077061cd46e4d3
sio:SIO_000628
miriam-gene:2271
,
lld:C0023269
;
a
sio:SIO_001122
.
}
dgn-np:NP151762.RAUHSCr6UmAR85qrWeoe2rDO1DFYzmAf3oxuB3FJbvTU0130_provenance
{
dgn-np:NP151762.RAUHSCr6UmAR85qrWeoe2rDO1DFYzmAf3oxuB3FJbvTU0130_assertion
dcterms:description
"[Although the familial occurrence of these rare tumors might be coincidental, it cannot be ruled out that, beside FH, mutations in another as yet unknown gene could give rise to both leiomyosarcoma and kidney 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:18986479
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP151762.RAUHSCr6UmAR85qrWeoe2rDO1DFYzmAf3oxuB3FJbvTU0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:20+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" .
}