@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP617692.RADnugrpCH-7NOOEJqBExLTmmmUPFRkW3Onc8Xsl-AxLE
> .
@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:NP617692.RADnugrpCH-7NOOEJqBExLTmmmUPFRkW3Onc8Xsl-AxLE130_head
{
this:
np:hasAssertion
dgn-np:NP617692.RADnugrpCH-7NOOEJqBExLTmmmUPFRkW3Onc8Xsl-AxLE130_assertion
;
np:hasProvenance
dgn-np:NP617692.RADnugrpCH-7NOOEJqBExLTmmmUPFRkW3Onc8Xsl-AxLE130_provenance
;
np:hasPublicationInfo
dgn-np:NP617692.RADnugrpCH-7NOOEJqBExLTmmmUPFRkW3Onc8Xsl-AxLE130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP617692.RADnugrpCH-7NOOEJqBExLTmmmUPFRkW3Onc8Xsl-AxLE130_assertion
a
np:Assertion
.
dgn-np:NP617692.RADnugrpCH-7NOOEJqBExLTmmmUPFRkW3Onc8Xsl-AxLE130_provenance
a
np:Provenance
.
dgn-np:NP617692.RADnugrpCH-7NOOEJqBExLTmmmUPFRkW3Onc8Xsl-AxLE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP617692.RADnugrpCH-7NOOEJqBExLTmmmUPFRkW3Onc8Xsl-AxLE130_assertion
{
miriam-gene:7249
a
ncit:C16612
.
lld:C0085548
a
ncit:C7057
.
dgn-gda:DGN8add896f824c81fd723d49117c3da022
sio:SIO_000628
miriam-gene:7249
,
lld:C0085548
;
a
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.
}
dgn-np:NP617692.RADnugrpCH-7NOOEJqBExLTmmmUPFRkW3Onc8Xsl-AxLE130_provenance
{
dgn-np:NP617692.RADnugrpCH-7NOOEJqBExLTmmmUPFRkW3Onc8Xsl-AxLE130_assertion
dcterms:description
"[Clinically, a small percentage of TSC patients develop severe infantile polycystic kidney disease (PKD), which is believed to be caused by deletion of the contiguous TSC2 and PKD1 genes on human chromosome 16.]. 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:19692352
;
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:NP617692.RADnugrpCH-7NOOEJqBExLTmmmUPFRkW3Onc8Xsl-AxLE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:13+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
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pav:authoredBy
<
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> , <
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> , <
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
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"v2.1.0" .
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