@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE
> .
@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:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_head
{
this:
np:hasAssertion
dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_assertion
;
np:hasProvenance
dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_provenance
;
np:hasPublicationInfo
dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_assertion
a
np:Assertion
.
dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_provenance
a
np:Provenance
.
dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0018552
a
ncit:C7057
.
dgn-gda:DGN241f84919306f0ac4f8b4f63df3332b5
sio:SIO_000628
miriam-gene:7248
,
lld:C0018552
;
a
sio:SIO_001121
.
}
dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_provenance
{
dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_assertion
dcterms:description
"[We have previously described in tuberous sclerosis (TSC) hamartomas the phenomenon of loss of heterozygosity (LOH) for DNA markers in the region of both the TSC2 gene on chromosome 16p13.3 and the TSC1 gene on 9q34.]. 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:8950679
;
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:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:22+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" .
}