@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ
> .
@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:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_head
{
this:
np:hasAssertion
dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_assertion
;
np:hasProvenance
dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_assertion
a
np:Assertion
.
dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_provenance
a
np:Provenance
.
dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_assertion
{
miriam-gene:4580
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN292e04bffe8d8f22295fd1f70ce86254
sio:SIO_000628
miriam-gene:4580
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_provenance
{
dgn-np:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_assertion
dcterms:description
"[Furthermore, analysis of FPGS transcripts in blood or bone marrow specimens from patients with acute lymphoblastic leukemia revealed exon 12 skipping, both at diagnosis and at relapse, the latter of which occurs after high-dose MTX-containing chemotherapy.]. 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:19131550
;
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:NP189563.RAWdJN0vXxDUM_NpsNyt87BFZaaweQLdwWlhhqElb7tFQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}