@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP560944.RAcqsd6hbuf2PftdFWQRQUt-r7QLZJHEGTR_a4d0WpGcM
> .
@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:NP560944.RAcqsd6hbuf2PftdFWQRQUt-r7QLZJHEGTR_a4d0WpGcM130_head
{
this:
np:hasAssertion
dgn-np:NP560944.RAcqsd6hbuf2PftdFWQRQUt-r7QLZJHEGTR_a4d0WpGcM130_assertion
;
np:hasProvenance
dgn-np:NP560944.RAcqsd6hbuf2PftdFWQRQUt-r7QLZJHEGTR_a4d0WpGcM130_provenance
;
np:hasPublicationInfo
dgn-np:NP560944.RAcqsd6hbuf2PftdFWQRQUt-r7QLZJHEGTR_a4d0WpGcM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP560944.RAcqsd6hbuf2PftdFWQRQUt-r7QLZJHEGTR_a4d0WpGcM130_assertion
a
np:Assertion
.
dgn-np:NP560944.RAcqsd6hbuf2PftdFWQRQUt-r7QLZJHEGTR_a4d0WpGcM130_provenance
a
np:Provenance
.
dgn-np:NP560944.RAcqsd6hbuf2PftdFWQRQUt-r7QLZJHEGTR_a4d0WpGcM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP560944.RAcqsd6hbuf2PftdFWQRQUt-r7QLZJHEGTR_a4d0WpGcM130_assertion
{
miriam-gene:5587
a
ncit:C16612
.
lld:C0751674
a
ncit:C7057
.
dgn-gda:DGNd04fae6281c65f356be6f6c4a48d526b
sio:SIO_000628
miriam-gene:5587
,
lld:C0751674
;
a
sio:SIO_001121
.
}
dgn-np:NP560944.RAcqsd6hbuf2PftdFWQRQUt-r7QLZJHEGTR_a4d0WpGcM130_provenance
{
dgn-np:NP560944.RAcqsd6hbuf2PftdFWQRQUt-r7QLZJHEGTR_a4d0WpGcM130_assertion
dcterms:description
"[Diffuse renal LAM lesions are presumed to generate multiple renal cysts by constricting the nephron rather than epithelial hyperplasia obstructing lumina, which is analysis of the TSC genes demonstrated that she did not have TSC2/PKD1 contiguous gene syndrome but had a TSC1 germline mutation (Sato T et al.]. 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:15257730
;
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:NP560944.RAcqsd6hbuf2PftdFWQRQUt-r7QLZJHEGTR_a4d0WpGcM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}