@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k
> .
@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:NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_head
{
this:
np:hasAssertion
dgn-np:NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_assertion
;
np:hasProvenance
dgn-np:NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_provenance
;
np:hasPublicationInfo
dgn-np:NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_assertion
a
np:Assertion
.
dgn-np:NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_provenance
a
np:Provenance
.
dgn-np:NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_assertion
{
miriam-gene:51741
a
ncit:C16612
.
lld:C0027708
a
ncit:C7057
.
dgn-gda:DGNe6ab3069ce1e107baf1b7b07e918def0
sio:SIO_000628
miriam-gene:51741
,
lld:C0027708
;
a
sio:SIO_001121
.
}
dgn-np:NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_provenance
{
dgn-np:NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_assertion
dcterms:description
"[The majority of chromosomes displayed uniparental disomies, and microdeletions were present in genes with known importance for tumor formation (LRP1B, FHIT, and WWOX) or organogenesis (NEGR1 and ZFPM2), abnormalities not previously reported for pediatric WT.]. 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:21947875
;
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:NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:56+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" .
}