@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o
> .
@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:NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_head
{
this:
np:hasAssertion
dgn-np:NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_assertion
;
np:hasProvenance
dgn-np:NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_provenance
;
np:hasPublicationInfo
dgn-np:NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_assertion
a
np:Assertion
.
dgn-np:NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_provenance
a
np:Provenance
.
dgn-np:NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_assertion
{
miriam-gene:23158
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGN2c9f7a667b81fcc53e5f9b46efb89d79
sio:SIO_000628
miriam-gene:23158
,
lld:C0023452
;
a
sio:SIO_001121
.
}
dgn-np:NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_provenance
{
dgn-np:NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_assertion
dcterms:description
"[To evaluate whether C3435T MDR1 polymorphism is associated with the occurrence and outcome of ALL, 113 children with ALL (median age 5.1 yr) and 175 healthy individuals of Polish Caucasian origin were studied by polymerase chain reaction-restriction fragment-length polymorphism (PCR-RFLP) assay.]. 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:15059065
;
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:NP738763.RAKdfydXWZg0WaLvbvhcLgWxkbh7R0GtL6eUViZ9lL1-o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:28+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" .
}