@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg
> .
@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:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_head
{
this:
np:hasAssertion
dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_assertion
;
np:hasProvenance
dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_provenance
;
np:hasPublicationInfo
dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_assertion
a
np:Assertion
.
dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_provenance
a
np:Provenance
.
dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0041341
a
ncit:C7057
.
dgn-gda:DGNf3738b8327ab1960057aef9b07c1652a
sio:SIO_000628
miriam-gene:7248
,
lld:C0041341
;
a
sio:SIO_001121
.
}
dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_provenance
{
dgn-np:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_assertion
dcterms:description
"[A proportion of hamartomas from patients with TSC show loss of heterozygosity (LOH) for DNA markers in the region of either the TSC1 gene on chromosome 9q34 or the TSC2 gene on 16p13.3.]. 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:8566961
;
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:NP1345988.RAS9BogrYP474P2VjOWRX_FAb1lrudzdvkFjuarrDfPwg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:56+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" .
}