@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP642083.RAW_ZnHMuzbzrDzSIjPS_EjaN5PZaBxTbBaWLacbvAZXw
> .
@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:NP642083.RAW_ZnHMuzbzrDzSIjPS_EjaN5PZaBxTbBaWLacbvAZXw130_head
{
this:
np:hasAssertion
dgn-np:NP642083.RAW_ZnHMuzbzrDzSIjPS_EjaN5PZaBxTbBaWLacbvAZXw130_assertion
;
np:hasProvenance
dgn-np:NP642083.RAW_ZnHMuzbzrDzSIjPS_EjaN5PZaBxTbBaWLacbvAZXw130_provenance
;
np:hasPublicationInfo
dgn-np:NP642083.RAW_ZnHMuzbzrDzSIjPS_EjaN5PZaBxTbBaWLacbvAZXw130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP642083.RAW_ZnHMuzbzrDzSIjPS_EjaN5PZaBxTbBaWLacbvAZXw130_assertion
a
np:Assertion
.
dgn-np:NP642083.RAW_ZnHMuzbzrDzSIjPS_EjaN5PZaBxTbBaWLacbvAZXw130_provenance
a
np:Provenance
.
dgn-np:NP642083.RAW_ZnHMuzbzrDzSIjPS_EjaN5PZaBxTbBaWLacbvAZXw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP642083.RAW_ZnHMuzbzrDzSIjPS_EjaN5PZaBxTbBaWLacbvAZXw130_assertion
{
miriam-gene:100188864
a
ncit:C16612
.
lld:C0003076
a
ncit:C7057
.
dgn-gda:DGN82010b09be09c2ebbf4c6cc9cc98e4a5
sio:SIO_000628
miriam-gene:100188864
,
lld:C0003076
;
a
sio:SIO_001121
.
}
dgn-np:NP642083.RAW_ZnHMuzbzrDzSIjPS_EjaN5PZaBxTbBaWLacbvAZXw130_provenance
{
dgn-np:NP642083.RAW_ZnHMuzbzrDzSIjPS_EjaN5PZaBxTbBaWLacbvAZXw130_assertion
dcterms:description
"[We attempted to determine whether all cases of AWTA (anirida-Wilms tumor association) or any of the following groups of patients show 11p deletion: cases of Wilms tumor with congenital abnormalities other than aniridia, those without any congenital abnormalities, tumor itself in cases of Wilms tumor without constitutional 11p deletion and cases of aniridia or hemihypertrophy without Wilms tumor.]. 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:NP642083.RAW_ZnHMuzbzrDzSIjPS_EjaN5PZaBxTbBaWLacbvAZXw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:27+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
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"v2.1.0" .
}