@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg
> .
@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:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_head
{
this:
np:hasAssertion
dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_assertion
;
np:hasProvenance
dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_provenance
;
np:hasPublicationInfo
dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_assertion
a
np:Assertion
.
dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_provenance
a
np:Provenance
.
dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_assertion
{
miriam-gene:4928
a
ncit:C16612
.
lld:C0033027
a
ncit:C7057
.
dgn-gda:DGNc276c0c22250f1815e388fc63b24ae17
sio:SIO_000628
miriam-gene:4928
,
lld:C0033027
;
a
sio:SIO_001121
.
}
dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_provenance
{
dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_assertion
dcterms:description
"[Using a NUP98-specific split-signal fluorescence in situ hybridization (FISH) probe combination, we analyzed 84 patients with acute myeloid leukemia (AML), acute lymphoblastic leukemia, or myelodysplastic syndrome with either normal karyotypes or 11p abnormalities to investigate whether there are unidentified 11p15 rearrangements.]. 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:16419055
;
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:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:18+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" .
}