@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP853652.RAhQsVjfdRRFgyKNSHkeIAdbKHRW5OLW3v3JwmeU3TvAg
> .
@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:NP853652.RAhQsVjfdRRFgyKNSHkeIAdbKHRW5OLW3v3JwmeU3TvAg130_head
{
this:
np:hasAssertion
dgn-np:NP853652.RAhQsVjfdRRFgyKNSHkeIAdbKHRW5OLW3v3JwmeU3TvAg130_assertion
;
np:hasProvenance
dgn-np:NP853652.RAhQsVjfdRRFgyKNSHkeIAdbKHRW5OLW3v3JwmeU3TvAg130_provenance
;
np:hasPublicationInfo
dgn-np:NP853652.RAhQsVjfdRRFgyKNSHkeIAdbKHRW5OLW3v3JwmeU3TvAg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP853652.RAhQsVjfdRRFgyKNSHkeIAdbKHRW5OLW3v3JwmeU3TvAg130_assertion
a
np:Assertion
.
dgn-np:NP853652.RAhQsVjfdRRFgyKNSHkeIAdbKHRW5OLW3v3JwmeU3TvAg130_provenance
a
np:Provenance
.
dgn-np:NP853652.RAhQsVjfdRRFgyKNSHkeIAdbKHRW5OLW3v3JwmeU3TvAg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP853652.RAhQsVjfdRRFgyKNSHkeIAdbKHRW5OLW3v3JwmeU3TvAg130_assertion
{
miriam-gene:3481
a
ncit:C16612
.
lld:C0432409
a
ncit:C7057
.
dgn-gda:DGNd68cc9d74f5d3564ac39351f89b03828
sio:SIO_000628
miriam-gene:3481
,
lld:C0432409
;
a
sio:SIO_001121
.
}
dgn-np:NP853652.RAhQsVjfdRRFgyKNSHkeIAdbKHRW5OLW3v3JwmeU3TvAg130_provenance
{
dgn-np:NP853652.RAhQsVjfdRRFgyKNSHkeIAdbKHRW5OLW3v3JwmeU3TvAg130_assertion
dcterms:description
"[We found no LOI in two cellular or mixed type tumors or in two classical type tumors, and concluded that the role of the LOI of IGF2 is not essential for the development and progression of CMN with or without trisomy 11.]. 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:12165445
;
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:NP853652.RAhQsVjfdRRFgyKNSHkeIAdbKHRW5OLW3v3JwmeU3TvAg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:42+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" .
}