@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_head
{
this:
np:hasAssertion
dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_assertion
;
np:hasProvenance
dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_provenance
;
np:hasPublicationInfo
dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_assertion
a
np:Assertion
.
dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_provenance
a
np:Provenance
.
dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0041341
a
ncit:C7057
.
dgn-gda:DGN9fbd2a07ea8b7a0bc93c8c38de15ec38
sio:SIO_000628
miriam-gene:7248
,
lld:C0041341
;
a
sio:SIO_001121
.
}
dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_provenance
{
dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_assertion
dcterms:description
"[Tuberous sclerosis complex (TSC) is an autosomal dominant disorder caused by mutations in either the TSC1 or the TSC2 genes and characterized by the development of benign hamartomatous growths in multiple organ systems.]. 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:15888477
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:29+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}