@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP569229.RAa154SuKFrcPNpWGZBS6iyjrkGiwZyoaAUChSoyFZu7M
> .
@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:NP569229.RAa154SuKFrcPNpWGZBS6iyjrkGiwZyoaAUChSoyFZu7M130_head
{
this:
np:hasAssertion
dgn-np:NP569229.RAa154SuKFrcPNpWGZBS6iyjrkGiwZyoaAUChSoyFZu7M130_assertion
;
np:hasProvenance
dgn-np:NP569229.RAa154SuKFrcPNpWGZBS6iyjrkGiwZyoaAUChSoyFZu7M130_provenance
;
np:hasPublicationInfo
dgn-np:NP569229.RAa154SuKFrcPNpWGZBS6iyjrkGiwZyoaAUChSoyFZu7M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP569229.RAa154SuKFrcPNpWGZBS6iyjrkGiwZyoaAUChSoyFZu7M130_assertion
a
np:Assertion
.
dgn-np:NP569229.RAa154SuKFrcPNpWGZBS6iyjrkGiwZyoaAUChSoyFZu7M130_provenance
a
np:Provenance
.
dgn-np:NP569229.RAa154SuKFrcPNpWGZBS6iyjrkGiwZyoaAUChSoyFZu7M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP569229.RAa154SuKFrcPNpWGZBS6iyjrkGiwZyoaAUChSoyFZu7M130_assertion
{
miriam-gene:6928
a
ncit:C16612
.
lld:C0403447
a
ncit:C7057
.
dgn-gda:DGNbe187bd5385a97a645440f4c843c4b74
sio:SIO_000628
miriam-gene:6928
,
lld:C0403447
;
a
sio:SIO_001121
.
}
dgn-np:NP569229.RAa154SuKFrcPNpWGZBS6iyjrkGiwZyoaAUChSoyFZu7M130_provenance
{
dgn-np:NP569229.RAa154SuKFrcPNpWGZBS6iyjrkGiwZyoaAUChSoyFZu7M130_assertion
dcterms:description
"[For estimation of the prevalence of these events, an unselected cohort of 99 unrelated patients with RHD that was associated with chronic renal insufficiency were screened for mutations in TCF2, PAX2, EYA1, SIX1, and SALL1.]. 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:16971658
;
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:NP569229.RAa154SuKFrcPNpWGZBS6iyjrkGiwZyoaAUChSoyFZu7M130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:03+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" .
}