@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP496752.RANP6vJ2QI9MAF_c-IziEN-RBNAh2ea7mO_iJ-raH8epk
> .
@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:NP496752.RANP6vJ2QI9MAF_c-IziEN-RBNAh2ea7mO_iJ-raH8epk130_head
{
this:
np:hasAssertion
dgn-np:NP496752.RANP6vJ2QI9MAF_c-IziEN-RBNAh2ea7mO_iJ-raH8epk130_assertion
;
np:hasProvenance
dgn-np:NP496752.RANP6vJ2QI9MAF_c-IziEN-RBNAh2ea7mO_iJ-raH8epk130_provenance
;
np:hasPublicationInfo
dgn-np:NP496752.RANP6vJ2QI9MAF_c-IziEN-RBNAh2ea7mO_iJ-raH8epk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP496752.RANP6vJ2QI9MAF_c-IziEN-RBNAh2ea7mO_iJ-raH8epk130_assertion
a
np:Assertion
.
dgn-np:NP496752.RANP6vJ2QI9MAF_c-IziEN-RBNAh2ea7mO_iJ-raH8epk130_provenance
a
np:Provenance
.
dgn-np:NP496752.RANP6vJ2QI9MAF_c-IziEN-RBNAh2ea7mO_iJ-raH8epk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP496752.RANP6vJ2QI9MAF_c-IziEN-RBNAh2ea7mO_iJ-raH8epk130_assertion
{
miriam-gene:100188864
a
ncit:C16612
.
lld:C0027708
a
ncit:C7057
.
dgn-gda:DGN0ae1e3dca33a3e4d0f05d2ebb884eccb
sio:SIO_000628
miriam-gene:100188864
,
lld:C0027708
;
a
sio:SIO_001121
.
}
dgn-np:NP496752.RANP6vJ2QI9MAF_c-IziEN-RBNAh2ea7mO_iJ-raH8epk130_provenance
{
dgn-np:NP496752.RANP6vJ2QI9MAF_c-IziEN-RBNAh2ea7mO_iJ-raH8epk130_assertion
dcterms:description
"[We studied a total of 29 index patients including five cases of AWTA, four cases of Wilms tumor with various congenital abnormalities, 16 cases of Wilms tumor without other abnormalities, three cases of aniridia in one of which Wilms tumor developed later and a case of hemihypertrophy.]. 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:6088386
;
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:NP496752.RANP6vJ2QI9MAF_c-IziEN-RBNAh2ea7mO_iJ-raH8epk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:56+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" .
}