@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI
> .
@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:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_head
{
this:
np:hasAssertion
dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_assertion
;
np:hasProvenance
dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_provenance
;
np:hasPublicationInfo
dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_assertion
a
np:Assertion
.
dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_provenance
a
np:Provenance
.
dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_assertion
{
miriam-gene:1056
a
ncit:C16612
.
lld:C0263662
a
ncit:C7057
.
dgn-gda:DGNc8e21becd663f07546bd9e6638d91d70
sio:SIO_000628
miriam-gene:1056
,
lld:C0263662
;
a
sio:SIO_001121
.
}
dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_provenance
{
dgn-np:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_assertion
dcterms:description
"[Histological investigation in 31 chronic myeloid leukemia (CML), 29 CMPDs not otherwise specified (CMPD-NOS), 28 essential thrombocytosis (ET), 15 polycythemia vera (PV) and three chronic eosinophilic leukemia/hypereosinophilic syndrome (CEL/HES) exhibited in 32% various amounts of lymphocytic infiltrate of sparsely to moderately diffuse or nodular types in the bone marrow, but the reactive or coinciding lymphomatous nature could not be revealed by histology alone in the majority of cases.]. 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:15257312
;
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:NP531674.RAqSMEsmvuDX7U_K53lGv39Rd7vC9LS8KjMUzGOILifWI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:21+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" .
}