@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA
> .
@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:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_head
{
this:
np:hasAssertion
dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_assertion
;
np:hasProvenance
dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_provenance
;
np:hasPublicationInfo
dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_assertion
a
np:Assertion
.
dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_provenance
a
np:Provenance
.
dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_assertion
{
miriam-gene:7249
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGN791cc767d0ed0e0eee357fea664da3c7
sio:SIO_000628
miriam-gene:7249
,
lld:C0022658
;
a
sio:SIO_001121
.
}
dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_provenance
{
dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_assertion
dcterms:description
"[We conducted a retrospective review of the clinical and radiographic records of 167 patients with tuberous sclerosis to determine the frequency of renal disease, the likelihood of significant renal morbidity, and the effects of genotype (TSC1 vs TSC2) and gender on renal phenotype.]. 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:17003820
;
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:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:19+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" .
}