@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP753237.RASwUkzXdisQSF-VE30zFz0uXkM1fF8jmI6P20nTgmQhA
> .
@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:NP753237.RASwUkzXdisQSF-VE30zFz0uXkM1fF8jmI6P20nTgmQhA130_head
{
this:
np:hasAssertion
dgn-np:NP753237.RASwUkzXdisQSF-VE30zFz0uXkM1fF8jmI6P20nTgmQhA130_assertion
;
np:hasProvenance
dgn-np:NP753237.RASwUkzXdisQSF-VE30zFz0uXkM1fF8jmI6P20nTgmQhA130_provenance
;
np:hasPublicationInfo
dgn-np:NP753237.RASwUkzXdisQSF-VE30zFz0uXkM1fF8jmI6P20nTgmQhA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP753237.RASwUkzXdisQSF-VE30zFz0uXkM1fF8jmI6P20nTgmQhA130_assertion
a
np:Assertion
.
dgn-np:NP753237.RASwUkzXdisQSF-VE30zFz0uXkM1fF8jmI6P20nTgmQhA130_provenance
a
np:Provenance
.
dgn-np:NP753237.RASwUkzXdisQSF-VE30zFz0uXkM1fF8jmI6P20nTgmQhA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP753237.RASwUkzXdisQSF-VE30zFz0uXkM1fF8jmI6P20nTgmQhA130_assertion
{
miriam-gene:4297
a
ncit:C16612
.
lld:C1297882
a
ncit:C7057
.
dgn-gda:DGNe8c810431a404c07230c9ef1cccc003e
sio:SIO_000628
miriam-gene:4297
,
lld:C1297882
;
a
sio:SIO_001121
.
}
dgn-np:NP753237.RASwUkzXdisQSF-VE30zFz0uXkM1fF8jmI6P20nTgmQhA130_provenance
{
dgn-np:NP753237.RASwUkzXdisQSF-VE30zFz0uXkM1fF8jmI6P20nTgmQhA130_assertion
dcterms:description
"[The amplification was presented as: amplification including only the 5' segment of the MLL gene (1 patient), trisomy 11 (3 patients), partial trisomy 11q (2 patients), isochromosome 11q (1 patient), and multiple amplification of specific regions (3 patients).]. 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:20471515
;
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:NP753237.RASwUkzXdisQSF-VE30zFz0uXkM1fF8jmI6P20nTgmQhA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}