@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY
> .
@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:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_head
{
this:
np:hasAssertion
dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_assertion
;
np:hasProvenance
dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_provenance
;
np:hasPublicationInfo
dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_assertion
a
np:Assertion
.
dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_provenance
a
np:Provenance
.
dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_assertion
{
miriam-gene:9244
a
ncit:C16612
.
lld:C0023487
a
ncit:C7057
.
dgn-gda:DGN41016afc48147277d8e3931435e84e0e
sio:SIO_000628
miriam-gene:9244
,
lld:C0023487
;
a
sio:SIO_001121
.
}
dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_provenance
{
dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_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:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:29+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" .
}