@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP597198.RAJxaF9F2mmmxzx6nJvd6nl1SP8y4nWKO5t52KegMIHB8
> .
@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:NP597198.RAJxaF9F2mmmxzx6nJvd6nl1SP8y4nWKO5t52KegMIHB8130_head
{
this:
np:hasAssertion
dgn-np:NP597198.RAJxaF9F2mmmxzx6nJvd6nl1SP8y4nWKO5t52KegMIHB8130_assertion
;
np:hasProvenance
dgn-np:NP597198.RAJxaF9F2mmmxzx6nJvd6nl1SP8y4nWKO5t52KegMIHB8130_provenance
;
np:hasPublicationInfo
dgn-np:NP597198.RAJxaF9F2mmmxzx6nJvd6nl1SP8y4nWKO5t52KegMIHB8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP597198.RAJxaF9F2mmmxzx6nJvd6nl1SP8y4nWKO5t52KegMIHB8130_assertion
a
np:Assertion
.
dgn-np:NP597198.RAJxaF9F2mmmxzx6nJvd6nl1SP8y4nWKO5t52KegMIHB8130_provenance
a
np:Provenance
.
dgn-np:NP597198.RAJxaF9F2mmmxzx6nJvd6nl1SP8y4nWKO5t52KegMIHB8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP597198.RAJxaF9F2mmmxzx6nJvd6nl1SP8y4nWKO5t52KegMIHB8130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGN11477d976a317cea71beed0b94694a4b
sio:SIO_000628
miriam-gene:7248
,
lld:C0022658
;
a
sio:SIO_001121
.
}
dgn-np:NP597198.RAJxaF9F2mmmxzx6nJvd6nl1SP8y4nWKO5t52KegMIHB8130_provenance
{
dgn-np:NP597198.RAJxaF9F2mmmxzx6nJvd6nl1SP8y4nWKO5t52KegMIHB8130_assertion
dcterms:description
"[Here, we will address the genetic, cellular and biochemical mechanisms that may contribute to the unusually broad spectrum of renal disease in cells with TSC1 or TSC2 mutations, and consider how the TSC signaling pathways may be linked to other renal diseases such as polycystic kidney disease and renal cell carcinoma.]. 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:15856327
;
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:NP597198.RAJxaF9F2mmmxzx6nJvd6nl1SP8y4nWKO5t52KegMIHB8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:59+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" .
}