@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP612136.RAFJXOlYOI9aHK43JHAOw0koRDG3GmEQ6n7YxlMqjcMAg
> .
@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:NP612136.RAFJXOlYOI9aHK43JHAOw0koRDG3GmEQ6n7YxlMqjcMAg130_head
{
this:
np:hasAssertion
dgn-np:NP612136.RAFJXOlYOI9aHK43JHAOw0koRDG3GmEQ6n7YxlMqjcMAg130_assertion
;
np:hasProvenance
dgn-np:NP612136.RAFJXOlYOI9aHK43JHAOw0koRDG3GmEQ6n7YxlMqjcMAg130_provenance
;
np:hasPublicationInfo
dgn-np:NP612136.RAFJXOlYOI9aHK43JHAOw0koRDG3GmEQ6n7YxlMqjcMAg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP612136.RAFJXOlYOI9aHK43JHAOw0koRDG3GmEQ6n7YxlMqjcMAg130_assertion
a
np:Assertion
.
dgn-np:NP612136.RAFJXOlYOI9aHK43JHAOw0koRDG3GmEQ6n7YxlMqjcMAg130_provenance
a
np:Provenance
.
dgn-np:NP612136.RAFJXOlYOI9aHK43JHAOw0koRDG3GmEQ6n7YxlMqjcMAg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP612136.RAFJXOlYOI9aHK43JHAOw0koRDG3GmEQ6n7YxlMqjcMAg130_assertion
{
miriam-gene:25
a
ncit:C16612
.
lld:C0023480
a
ncit:C7057
.
dgn-gda:DGN3b6e59380294d41f4119f8166a762343
sio:SIO_000628
miriam-gene:25
,
lld:C0023480
;
a
sio:SIO_001121
.
}
dgn-np:NP612136.RAFJXOlYOI9aHK43JHAOw0koRDG3GmEQ6n7YxlMqjcMAg130_provenance
{
dgn-np:NP612136.RAFJXOlYOI9aHK43JHAOw0koRDG3GmEQ6n7YxlMqjcMAg130_assertion
dcterms:description
"[However, because of its unique biological characteristics such as absolute monocytosis with dysplasia, absence of Philadelphia chromosome or BCR-ABL fusion protein, hypergammaglobulinaemia and raised fetal haemoglobin level, this disorder does not satisfy the criteria for inclusion in the CML or chronic myelomonocytic leukaemia (CMML) group, as seen in adult patients.]. 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:20514855
;
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:NP612136.RAFJXOlYOI9aHK43JHAOw0koRDG3GmEQ6n7YxlMqjcMAg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:10+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" .
}