@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP897762.RA2beEWyyV5Fqm0XRcswcAXPE1rHaETku0O5nYB9dJo5A
> .
@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:NP897762.RA2beEWyyV5Fqm0XRcswcAXPE1rHaETku0O5nYB9dJo5A130_head
{
this:
np:hasAssertion
dgn-np:NP897762.RA2beEWyyV5Fqm0XRcswcAXPE1rHaETku0O5nYB9dJo5A130_assertion
;
np:hasProvenance
dgn-np:NP897762.RA2beEWyyV5Fqm0XRcswcAXPE1rHaETku0O5nYB9dJo5A130_provenance
;
np:hasPublicationInfo
dgn-np:NP897762.RA2beEWyyV5Fqm0XRcswcAXPE1rHaETku0O5nYB9dJo5A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP897762.RA2beEWyyV5Fqm0XRcswcAXPE1rHaETku0O5nYB9dJo5A130_assertion
a
np:Assertion
.
dgn-np:NP897762.RA2beEWyyV5Fqm0XRcswcAXPE1rHaETku0O5nYB9dJo5A130_provenance
a
np:Provenance
.
dgn-np:NP897762.RA2beEWyyV5Fqm0XRcswcAXPE1rHaETku0O5nYB9dJo5A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP897762.RA2beEWyyV5Fqm0XRcswcAXPE1rHaETku0O5nYB9dJo5A130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGNcab4c5d140601e351428545e51cd9df7
sio:SIO_000628
miriam-gene:7248
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP897762.RA2beEWyyV5Fqm0XRcswcAXPE1rHaETku0O5nYB9dJo5A130_provenance
{
dgn-np:NP897762.RA2beEWyyV5Fqm0XRcswcAXPE1rHaETku0O5nYB9dJo5A130_assertion
dcterms:description
"[This study aims to describe the phenotypic and genotypic characteristics of 45 Australian patients with tuberous sclerosis complex (TSC), to assess risk factors for intellectual disability, to compare patients with TSC1 and TSC2 mutations and to assess adherence to surveillance recommendations.]. 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:21449900
;
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:NP897762.RA2beEWyyV5Fqm0XRcswcAXPE1rHaETku0O5nYB9dJo5A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:12+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" .
}