@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP321717.RAQ-0lRN9ipXPcYCYU_cuetjfnM68Ua7RC1FsgwGGXCEw
> .
@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:NP321717.RAQ-0lRN9ipXPcYCYU_cuetjfnM68Ua7RC1FsgwGGXCEw130_head
{
this:
np:hasAssertion
dgn-np:NP321717.RAQ-0lRN9ipXPcYCYU_cuetjfnM68Ua7RC1FsgwGGXCEw130_assertion
;
np:hasProvenance
dgn-np:NP321717.RAQ-0lRN9ipXPcYCYU_cuetjfnM68Ua7RC1FsgwGGXCEw130_provenance
;
np:hasPublicationInfo
dgn-np:NP321717.RAQ-0lRN9ipXPcYCYU_cuetjfnM68Ua7RC1FsgwGGXCEw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP321717.RAQ-0lRN9ipXPcYCYU_cuetjfnM68Ua7RC1FsgwGGXCEw130_assertion
a
np:Assertion
.
dgn-np:NP321717.RAQ-0lRN9ipXPcYCYU_cuetjfnM68Ua7RC1FsgwGGXCEw130_provenance
a
np:Provenance
.
dgn-np:NP321717.RAQ-0lRN9ipXPcYCYU_cuetjfnM68Ua7RC1FsgwGGXCEw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP321717.RAQ-0lRN9ipXPcYCYU_cuetjfnM68Ua7RC1FsgwGGXCEw130_assertion
{
miriam-gene:613
a
ncit:C16612
.
lld:C0085669
a
ncit:C7057
.
dgn-gda:DGNe5c8dbe0748a480cdce41b96b62a6444
sio:SIO_000628
miriam-gene:613
,
lld:C0085669
;
a
sio:SIO_001121
.
}
dgn-np:NP321717.RAQ-0lRN9ipXPcYCYU_cuetjfnM68Ua7RC1FsgwGGXCEw130_provenance
{
dgn-np:NP321717.RAQ-0lRN9ipXPcYCYU_cuetjfnM68Ua7RC1FsgwGGXCEw130_assertion
dcterms:description
"[The main differences relate to the presence of Ph-negative metaphases at diagnosis and the disappearance of Ph in complete remission in acute leukemia, and the localization of the chromosome breakpoints in the BCR gene, in the bcr segment in chronic leukemia and in the first intron of the BCR gene in 50% of acute leukemias.]. 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:8251902
;
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:NP321717.RAQ-0lRN9ipXPcYCYU_cuetjfnM68Ua7RC1FsgwGGXCEw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:06+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" .
}