@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP502935.RAr2F-P4HLjbJ9NUmYgPF8HQb71tYovC8sR8L8-bM23cQ
> .
@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:NP502935.RAr2F-P4HLjbJ9NUmYgPF8HQb71tYovC8sR8L8-bM23cQ130_head
{
this:
np:hasAssertion
dgn-np:NP502935.RAr2F-P4HLjbJ9NUmYgPF8HQb71tYovC8sR8L8-bM23cQ130_assertion
;
np:hasProvenance
dgn-np:NP502935.RAr2F-P4HLjbJ9NUmYgPF8HQb71tYovC8sR8L8-bM23cQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP502935.RAr2F-P4HLjbJ9NUmYgPF8HQb71tYovC8sR8L8-bM23cQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP502935.RAr2F-P4HLjbJ9NUmYgPF8HQb71tYovC8sR8L8-bM23cQ130_assertion
a
np:Assertion
.
dgn-np:NP502935.RAr2F-P4HLjbJ9NUmYgPF8HQb71tYovC8sR8L8-bM23cQ130_provenance
a
np:Provenance
.
dgn-np:NP502935.RAr2F-P4HLjbJ9NUmYgPF8HQb71tYovC8sR8L8-bM23cQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP502935.RAr2F-P4HLjbJ9NUmYgPF8HQb71tYovC8sR8L8-bM23cQ130_assertion
{
miriam-gene:9244
a
ncit:C16612
.
lld:C0432412
a
ncit:C7057
.
dgn-gda:DGN8dd00236b873fd4ea8f7bdb482293ede
sio:SIO_000628
miriam-gene:9244
,
lld:C0432412
;
a
sio:SIO_001121
.
}
dgn-np:NP502935.RAr2F-P4HLjbJ9NUmYgPF8HQb71tYovC8sR8L8-bM23cQ130_provenance
{
dgn-np:NP502935.RAr2F-P4HLjbJ9NUmYgPF8HQb71tYovC8sR8L8-bM23cQ130_assertion
dcterms:description
"[Chromosomal in situ suppression (CISS) hybridization was performed with library DNA from sorted human chromosomes 8, 9, 15, 17, 21, and 22 on immunologically stained bone marrow cells of four patients with a hematologic neoplasm, including two patients with myelodysplastic syndrome and trisomy 8, one patient with promyelocytic leukemia bearing the translocation t(15;17)(q22;q11-12), and one patient with chronic myeloid leukemia and the translocation t(9;22)(q34;q11).]. 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:1373313
;
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:NP502935.RAr2F-P4HLjbJ9NUmYgPF8HQb71tYovC8sR8L8-bM23cQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:59+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" .
}