@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP190688.RAfER_P6GOPhk8tlfuVFXME8fkWy-4mD-IdIjh-7FBCKo
> .
@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:NP190688.RAfER_P6GOPhk8tlfuVFXME8fkWy-4mD-IdIjh-7FBCKo130_head
{
this:
np:hasAssertion
dgn-np:NP190688.RAfER_P6GOPhk8tlfuVFXME8fkWy-4mD-IdIjh-7FBCKo130_assertion
;
np:hasProvenance
dgn-np:NP190688.RAfER_P6GOPhk8tlfuVFXME8fkWy-4mD-IdIjh-7FBCKo130_provenance
;
np:hasPublicationInfo
dgn-np:NP190688.RAfER_P6GOPhk8tlfuVFXME8fkWy-4mD-IdIjh-7FBCKo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP190688.RAfER_P6GOPhk8tlfuVFXME8fkWy-4mD-IdIjh-7FBCKo130_assertion
a
np:Assertion
.
dgn-np:NP190688.RAfER_P6GOPhk8tlfuVFXME8fkWy-4mD-IdIjh-7FBCKo130_provenance
a
np:Provenance
.
dgn-np:NP190688.RAfER_P6GOPhk8tlfuVFXME8fkWy-4mD-IdIjh-7FBCKo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP190688.RAfER_P6GOPhk8tlfuVFXME8fkWy-4mD-IdIjh-7FBCKo130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0027627
a
ncit:C7057
.
dgn-gda:DGN48976b1e5ec67d9bafe57082d80805a5
sio:SIO_000628
miriam-gene:7248
,
lld:C0027627
;
a
sio:SIO_001121
.
}
dgn-np:NP190688.RAfER_P6GOPhk8tlfuVFXME8fkWy-4mD-IdIjh-7FBCKo130_provenance
{
dgn-np:NP190688.RAfER_P6GOPhk8tlfuVFXME8fkWy-4mD-IdIjh-7FBCKo130_assertion
dcterms:description
"[Two of the most unusual phenotypes in TSC are the apparent metastasis of benign cells carrying TSC1 and TSC2 mutations, resulting in pulmonary lymphangiomyomatosis, and the ability of cells with TSC1 or TSC2 mutations to differentiate into the separate components of renal angiomyolipomas (vessels, smooth muscle and fat).]. 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:16288294
;
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:NP190688.RAfER_P6GOPhk8tlfuVFXME8fkWy-4mD-IdIjh-7FBCKo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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" .
}