@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP368043.RAd5rgNLLfnPi8fUeCiUSscCqnc7GNIh9xJKKAoMBp478
> .
@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:NP368043.RAd5rgNLLfnPi8fUeCiUSscCqnc7GNIh9xJKKAoMBp478130_head
{
this:
np:hasAssertion
dgn-np:NP368043.RAd5rgNLLfnPi8fUeCiUSscCqnc7GNIh9xJKKAoMBp478130_assertion
;
np:hasProvenance
dgn-np:NP368043.RAd5rgNLLfnPi8fUeCiUSscCqnc7GNIh9xJKKAoMBp478130_provenance
;
np:hasPublicationInfo
dgn-np:NP368043.RAd5rgNLLfnPi8fUeCiUSscCqnc7GNIh9xJKKAoMBp478130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP368043.RAd5rgNLLfnPi8fUeCiUSscCqnc7GNIh9xJKKAoMBp478130_assertion
a
np:Assertion
.
dgn-np:NP368043.RAd5rgNLLfnPi8fUeCiUSscCqnc7GNIh9xJKKAoMBp478130_provenance
a
np:Provenance
.
dgn-np:NP368043.RAd5rgNLLfnPi8fUeCiUSscCqnc7GNIh9xJKKAoMBp478130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP368043.RAd5rgNLLfnPi8fUeCiUSscCqnc7GNIh9xJKKAoMBp478130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0036572
a
ncit:C7057
.
dgn-gda:DGN07a24e74fccd7218a94272e4d2597938
sio:SIO_000628
miriam-gene:7248
,
lld:C0036572
;
a
sio:SIO_001121
.
}
dgn-np:NP368043.RAd5rgNLLfnPi8fUeCiUSscCqnc7GNIh9xJKKAoMBp478130_provenance
{
dgn-np:NP368043.RAd5rgNLLfnPi8fUeCiUSscCqnc7GNIh9xJKKAoMBp478130_assertion
dcterms:description
"[While these malformations are believed to result from the effects of TSC1 or TSC2 gene mutations, the molecular mechanisms leading to tuber formation, as well as the onset of seizures, remain largely unknown.]. 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:19912235
;
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:NP368043.RAd5rgNLLfnPi8fUeCiUSscCqnc7GNIh9xJKKAoMBp478130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:35+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" .
}