@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP568792.RABrJ7Xc2Hp1Uz_lZKlVZ21-h_a3o9gB4L2NaeQiK6CEk
> .
@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:NP568792.RABrJ7Xc2Hp1Uz_lZKlVZ21-h_a3o9gB4L2NaeQiK6CEk130_head
{
this:
np:hasAssertion
dgn-np:NP568792.RABrJ7Xc2Hp1Uz_lZKlVZ21-h_a3o9gB4L2NaeQiK6CEk130_assertion
;
np:hasProvenance
dgn-np:NP568792.RABrJ7Xc2Hp1Uz_lZKlVZ21-h_a3o9gB4L2NaeQiK6CEk130_provenance
;
np:hasPublicationInfo
dgn-np:NP568792.RABrJ7Xc2Hp1Uz_lZKlVZ21-h_a3o9gB4L2NaeQiK6CEk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP568792.RABrJ7Xc2Hp1Uz_lZKlVZ21-h_a3o9gB4L2NaeQiK6CEk130_assertion
a
np:Assertion
.
dgn-np:NP568792.RABrJ7Xc2Hp1Uz_lZKlVZ21-h_a3o9gB4L2NaeQiK6CEk130_provenance
a
np:Provenance
.
dgn-np:NP568792.RABrJ7Xc2Hp1Uz_lZKlVZ21-h_a3o9gB4L2NaeQiK6CEk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP568792.RABrJ7Xc2Hp1Uz_lZKlVZ21-h_a3o9gB4L2NaeQiK6CEk130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C1762616
a
ncit:C7057
.
dgn-gda:DGNf6873c526be5bd63e31bbee1709c021c
sio:SIO_000628
miriam-gene:7248
,
lld:C1762616
;
a
sio:SIO_001121
.
}
dgn-np:NP568792.RABrJ7Xc2Hp1Uz_lZKlVZ21-h_a3o9gB4L2NaeQiK6CEk130_provenance
{
dgn-np:NP568792.RABrJ7Xc2Hp1Uz_lZKlVZ21-h_a3o9gB4L2NaeQiK6CEk130_assertion
dcterms:description
"[The types of malignancy reported in carriers of constitutional ring chromosomes r(11), r(13), and r(22) are concordant with the chromosomal assignment of tumour suppressor loci associated with Wilms' tumour, retinoblastoma, and meningioma.]. 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:1336057
;
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:NP568792.RABrJ7Xc2Hp1Uz_lZKlVZ21-h_a3o9gB4L2NaeQiK6CEk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:43+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" .
}