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http://rdf.disgenet.org/nanopublications.trig#NP462794.RAMrpeqcIKFcKaRSbmMmkxyIPnApgQWYaAqHFyzPTEPoE
> .
@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:NP462794.RAMrpeqcIKFcKaRSbmMmkxyIPnApgQWYaAqHFyzPTEPoE130_head
{
this:
np:hasAssertion
dgn-np:NP462794.RAMrpeqcIKFcKaRSbmMmkxyIPnApgQWYaAqHFyzPTEPoE130_assertion
;
np:hasProvenance
dgn-np:NP462794.RAMrpeqcIKFcKaRSbmMmkxyIPnApgQWYaAqHFyzPTEPoE130_provenance
;
np:hasPublicationInfo
dgn-np:NP462794.RAMrpeqcIKFcKaRSbmMmkxyIPnApgQWYaAqHFyzPTEPoE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP462794.RAMrpeqcIKFcKaRSbmMmkxyIPnApgQWYaAqHFyzPTEPoE130_assertion
a
np:Assertion
.
dgn-np:NP462794.RAMrpeqcIKFcKaRSbmMmkxyIPnApgQWYaAqHFyzPTEPoE130_provenance
a
np:Provenance
.
dgn-np:NP462794.RAMrpeqcIKFcKaRSbmMmkxyIPnApgQWYaAqHFyzPTEPoE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP462794.RAMrpeqcIKFcKaRSbmMmkxyIPnApgQWYaAqHFyzPTEPoE130_assertion
{
miriam-gene:84159
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGNc7d6da6f828617d4ca35b497b44f3762
sio:SIO_000628
miriam-gene:84159
,
lld:C0023452
;
a
sio:SIO_001121
.
}
dgn-np:NP462794.RAMrpeqcIKFcKaRSbmMmkxyIPnApgQWYaAqHFyzPTEPoE130_provenance
{
dgn-np:NP462794.RAMrpeqcIKFcKaRSbmMmkxyIPnApgQWYaAqHFyzPTEPoE130_assertion
dcterms:description
"[Recent studies have shown that SNPs mapping to 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B), and 14q11.2 (CEBPE) and carrier status for recessively inherited Nijmegen Breakage syndrome (NBS) influence childhood acute lymphoblastic leukemia (ALL) risk.]. 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:21889209
;
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:NP462794.RAMrpeqcIKFcKaRSbmMmkxyIPnApgQWYaAqHFyzPTEPoE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:35+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" .
}