@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP618202.RAXITj4GzyRjyCA4tH6-8PYUhgWSntN4lWdCs9F9pvjJg
> .
@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:NP618202.RAXITj4GzyRjyCA4tH6-8PYUhgWSntN4lWdCs9F9pvjJg130_head
{
this:
np:hasAssertion
dgn-np:NP618202.RAXITj4GzyRjyCA4tH6-8PYUhgWSntN4lWdCs9F9pvjJg130_assertion
;
np:hasProvenance
dgn-np:NP618202.RAXITj4GzyRjyCA4tH6-8PYUhgWSntN4lWdCs9F9pvjJg130_provenance
;
np:hasPublicationInfo
dgn-np:NP618202.RAXITj4GzyRjyCA4tH6-8PYUhgWSntN4lWdCs9F9pvjJg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP618202.RAXITj4GzyRjyCA4tH6-8PYUhgWSntN4lWdCs9F9pvjJg130_assertion
a
np:Assertion
.
dgn-np:NP618202.RAXITj4GzyRjyCA4tH6-8PYUhgWSntN4lWdCs9F9pvjJg130_provenance
a
np:Provenance
.
dgn-np:NP618202.RAXITj4GzyRjyCA4tH6-8PYUhgWSntN4lWdCs9F9pvjJg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP618202.RAXITj4GzyRjyCA4tH6-8PYUhgWSntN4lWdCs9F9pvjJg130_assertion
{
miriam-gene:613
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGNb1e01979f819c036dd4d9388cf86ece1
sio:SIO_000628
miriam-gene:613
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP618202.RAXITj4GzyRjyCA4tH6-8PYUhgWSntN4lWdCs9F9pvjJg130_provenance
{
dgn-np:NP618202.RAXITj4GzyRjyCA4tH6-8PYUhgWSntN4lWdCs9F9pvjJg130_assertion
dcterms:description
"[In this respect, the rather clear description of CML in cytogenetic, clinical, and laboratory terms, the relatively long chronic phase of the disease, and the association of the blastic phase with nonrandom chromosome changes (at least in the initial phases of the disease) make Ph-positive CML an excellent candidate for a model for the study of molecular events in human neoplasia.]. 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:3004697
;
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:NP618202.RAXITj4GzyRjyCA4tH6-8PYUhgWSntN4lWdCs9F9pvjJg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:13+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" .
}