@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP712706.RAdcj3V1xVNNO3LMi0VMRYnCo6DFLcznw6ptLVF1q1U-o
> .
@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:NP712706.RAdcj3V1xVNNO3LMi0VMRYnCo6DFLcznw6ptLVF1q1U-o130_head
{
this:
np:hasAssertion
dgn-np:NP712706.RAdcj3V1xVNNO3LMi0VMRYnCo6DFLcznw6ptLVF1q1U-o130_assertion
;
np:hasProvenance
dgn-np:NP712706.RAdcj3V1xVNNO3LMi0VMRYnCo6DFLcznw6ptLVF1q1U-o130_provenance
;
np:hasPublicationInfo
dgn-np:NP712706.RAdcj3V1xVNNO3LMi0VMRYnCo6DFLcznw6ptLVF1q1U-o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP712706.RAdcj3V1xVNNO3LMi0VMRYnCo6DFLcznw6ptLVF1q1U-o130_assertion
a
np:Assertion
.
dgn-np:NP712706.RAdcj3V1xVNNO3LMi0VMRYnCo6DFLcznw6ptLVF1q1U-o130_provenance
a
np:Provenance
.
dgn-np:NP712706.RAdcj3V1xVNNO3LMi0VMRYnCo6DFLcznw6ptLVF1q1U-o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP712706.RAdcj3V1xVNNO3LMi0VMRYnCo6DFLcznw6ptLVF1q1U-o130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0018939
a
ncit:C7057
.
dgn-gda:DGN1158bb36daf68277927ec97c1bd700dc
sio:SIO_000628
miriam-gene:3342
,
lld:C0018939
;
a
sio:SIO_001121
.
}
dgn-np:NP712706.RAdcj3V1xVNNO3LMi0VMRYnCo6DFLcznw6ptLVF1q1U-o130_provenance
{
dgn-np:NP712706.RAdcj3V1xVNNO3LMi0VMRYnCo6DFLcznw6ptLVF1q1U-o130_assertion
dcterms:description
"[For this purpose, bone marrow aspirates of 33 patients with different hematologic disorders were examined with CGH and the results compared with conventional cytogenetics (CC) and fluorescence in situ hybridization (FISH).]. 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:9712425
;
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:NP712706.RAdcj3V1xVNNO3LMi0VMRYnCo6DFLcznw6ptLVF1q1U-o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:13+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" .
}