@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1152495.RAhxXyLdVGTXaPpQ35jFzDP_CqFAha7BPWo7h7j1d4DOQ
> .
@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:NP1152495.RAhxXyLdVGTXaPpQ35jFzDP_CqFAha7BPWo7h7j1d4DOQ130_head
{
this:
np:hasAssertion
dgn-np:NP1152495.RAhxXyLdVGTXaPpQ35jFzDP_CqFAha7BPWo7h7j1d4DOQ130_assertion
;
np:hasProvenance
dgn-np:NP1152495.RAhxXyLdVGTXaPpQ35jFzDP_CqFAha7BPWo7h7j1d4DOQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP1152495.RAhxXyLdVGTXaPpQ35jFzDP_CqFAha7BPWo7h7j1d4DOQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1152495.RAhxXyLdVGTXaPpQ35jFzDP_CqFAha7BPWo7h7j1d4DOQ130_assertion
a
np:Assertion
.
dgn-np:NP1152495.RAhxXyLdVGTXaPpQ35jFzDP_CqFAha7BPWo7h7j1d4DOQ130_provenance
a
np:Provenance
.
dgn-np:NP1152495.RAhxXyLdVGTXaPpQ35jFzDP_CqFAha7BPWo7h7j1d4DOQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1152495.RAhxXyLdVGTXaPpQ35jFzDP_CqFAha7BPWo7h7j1d4DOQ130_assertion
{
miriam-gene:51196
a
ncit:C16612
.
lld:C0017668
a
ncit:C7057
.
dgn-gda:DGNef76878db73260d3c45f1e4835e6af17
sio:SIO_000628
miriam-gene:51196
,
lld:C0017668
;
a
sio:SIO_001121
.
}
dgn-np:NP1152495.RAhxXyLdVGTXaPpQ35jFzDP_CqFAha7BPWo7h7j1d4DOQ130_provenance
{
dgn-np:NP1152495.RAhxXyLdVGTXaPpQ35jFzDP_CqFAha7BPWo7h7j1d4DOQ130_assertion
dcterms:description
"[The prevalence of pathogenic mutations in five genes (NPHS2, TRPC6, ACTN4, INF2 and PLCE1) and of APOL1 risk alleles (G1 and G2) was ascertained in children and adults diagnosed between 1984 and 2011 with FSGS by renal biopsy.]. 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:24500309
;
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:NP1152495.RAhxXyLdVGTXaPpQ35jFzDP_CqFAha7BPWo7h7j1d4DOQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:28+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" .
}