@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP236496.RA2LTuFtRPQVOWlHQxoJh2wMFw8M9ba9EtLtB-hLrI-XI
> .
@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:NP236496.RA2LTuFtRPQVOWlHQxoJh2wMFw8M9ba9EtLtB-hLrI-XI130_head
{
this:
np:hasAssertion
dgn-np:NP236496.RA2LTuFtRPQVOWlHQxoJh2wMFw8M9ba9EtLtB-hLrI-XI130_assertion
;
np:hasProvenance
dgn-np:NP236496.RA2LTuFtRPQVOWlHQxoJh2wMFw8M9ba9EtLtB-hLrI-XI130_provenance
;
np:hasPublicationInfo
dgn-np:NP236496.RA2LTuFtRPQVOWlHQxoJh2wMFw8M9ba9EtLtB-hLrI-XI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP236496.RA2LTuFtRPQVOWlHQxoJh2wMFw8M9ba9EtLtB-hLrI-XI130_assertion
a
np:Assertion
.
dgn-np:NP236496.RA2LTuFtRPQVOWlHQxoJh2wMFw8M9ba9EtLtB-hLrI-XI130_provenance
a
np:Provenance
.
dgn-np:NP236496.RA2LTuFtRPQVOWlHQxoJh2wMFw8M9ba9EtLtB-hLrI-XI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP236496.RA2LTuFtRPQVOWlHQxoJh2wMFw8M9ba9EtLtB-hLrI-XI130_assertion
{
miriam-gene:5551
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN569fdd6fee35620cdcbc4da62d5295a1
sio:SIO_000628
miriam-gene:5551
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP236496.RA2LTuFtRPQVOWlHQxoJh2wMFw8M9ba9EtLtB-hLrI-XI130_provenance
{
dgn-np:NP236496.RA2LTuFtRPQVOWlHQxoJh2wMFw8M9ba9EtLtB-hLrI-XI130_assertion
dcterms:description
"[To address whether mutations and single nucleotide polymorphisms (SNPs) in perforin gene (PRF1) are correlated with acute lymphoblastic leukemia (ALL) in Chinese, we screened mutations in codon region of PRF1 in 111 ALL patients, and correlated the results with patients' immunophenotype, karyotype and fusion genes.]. 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:20638125
;
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:NP236496.RA2LTuFtRPQVOWlHQxoJh2wMFw8M9ba9EtLtB-hLrI-XI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:12+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" .
}