@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP671032.RAU4Wphj3nWS9VgE9t_9S284jisGRLVia2G1mMu6G571M
> .
@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:NP671032.RAU4Wphj3nWS9VgE9t_9S284jisGRLVia2G1mMu6G571M130_head
{
this:
np:hasAssertion
dgn-np:NP671032.RAU4Wphj3nWS9VgE9t_9S284jisGRLVia2G1mMu6G571M130_assertion
;
np:hasProvenance
dgn-np:NP671032.RAU4Wphj3nWS9VgE9t_9S284jisGRLVia2G1mMu6G571M130_provenance
;
np:hasPublicationInfo
dgn-np:NP671032.RAU4Wphj3nWS9VgE9t_9S284jisGRLVia2G1mMu6G571M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP671032.RAU4Wphj3nWS9VgE9t_9S284jisGRLVia2G1mMu6G571M130_assertion
a
np:Assertion
.
dgn-np:NP671032.RAU4Wphj3nWS9VgE9t_9S284jisGRLVia2G1mMu6G571M130_provenance
a
np:Provenance
.
dgn-np:NP671032.RAU4Wphj3nWS9VgE9t_9S284jisGRLVia2G1mMu6G571M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP671032.RAU4Wphj3nWS9VgE9t_9S284jisGRLVia2G1mMu6G571M130_assertion
{
miriam-gene:8170
a
ncit:C16612
.
lld:C0027627
a
ncit:C7057
.
dgn-gda:DGN374dbeb1bffb1d17ee20273ab933a2cf
sio:SIO_000628
miriam-gene:8170
,
lld:C0027627
;
a
sio:SIO_001121
.
}
dgn-np:NP671032.RAU4Wphj3nWS9VgE9t_9S284jisGRLVia2G1mMu6G571M130_provenance
{
dgn-np:NP671032.RAU4Wphj3nWS9VgE9t_9S284jisGRLVia2G1mMu6G571M130_assertion
dcterms:description
"[Genetic polymorphisms in the 3'UTR region of the CXCL12 (rs1801157) and TP53 codon 72 (rs1042522) genes may contribute to susceptibility to childhood ALL because they affect some important processes, such as metastasis regulation and tumor suppression.]. 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:23653000
;
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:NP671032.RAU4Wphj3nWS9VgE9t_9S284jisGRLVia2G1mMu6G571M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:45+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" .
}