@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP273902.RApLembC4B4iXSjMkXcL2pU4-hiHmRJpvSoWfr8kWiAMk
> .
@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:NP273902.RApLembC4B4iXSjMkXcL2pU4-hiHmRJpvSoWfr8kWiAMk130_head
{
this:
np:hasAssertion
dgn-np:NP273902.RApLembC4B4iXSjMkXcL2pU4-hiHmRJpvSoWfr8kWiAMk130_assertion
;
np:hasProvenance
dgn-np:NP273902.RApLembC4B4iXSjMkXcL2pU4-hiHmRJpvSoWfr8kWiAMk130_provenance
;
np:hasPublicationInfo
dgn-np:NP273902.RApLembC4B4iXSjMkXcL2pU4-hiHmRJpvSoWfr8kWiAMk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP273902.RApLembC4B4iXSjMkXcL2pU4-hiHmRJpvSoWfr8kWiAMk130_assertion
a
np:Assertion
.
dgn-np:NP273902.RApLembC4B4iXSjMkXcL2pU4-hiHmRJpvSoWfr8kWiAMk130_provenance
a
np:Provenance
.
dgn-np:NP273902.RApLembC4B4iXSjMkXcL2pU4-hiHmRJpvSoWfr8kWiAMk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP273902.RApLembC4B4iXSjMkXcL2pU4-hiHmRJpvSoWfr8kWiAMk130_assertion
{
miriam-gene:613
a
ncit:C16612
.
lld:C0279549
a
ncit:C7057
.
dgn-gda:DGNa2ff1ad42654a3e0c058a07c3ed1fdb2
sio:SIO_000628
miriam-gene:613
,
lld:C0279549
;
a
sio:SIO_001121
.
}
dgn-np:NP273902.RApLembC4B4iXSjMkXcL2pU4-hiHmRJpvSoWfr8kWiAMk130_provenance
{
dgn-np:NP273902.RApLembC4B4iXSjMkXcL2pU4-hiHmRJpvSoWfr8kWiAMk130_assertion
dcterms:description
"[Philadelphia (Ph) chromosome negative chronic myeloid leukemia (CML) can be distinguished from clinically similar disorders on the basis of the presence of rearrangement of the breakpoint cluster region (bcr) of chromosome 22.]. 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:3180023
;
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:NP273902.RApLembC4B4iXSjMkXcL2pU4-hiHmRJpvSoWfr8kWiAMk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:34+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" .
}