@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_head
{
this:
np:hasAssertion
dgn-np:NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_assertion
;
np:hasProvenance
dgn-np:NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_provenance
;
np:hasPublicationInfo
dgn-np:NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_assertion
a
np:Assertion
.
dgn-np:NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_provenance
a
np:Provenance
.
dgn-np:NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_assertion
{
miriam-gene:5243
a
ncit:C16612
.
lld:C0023448
a
ncit:C7057
.
dgn-gda:DGN9e1a346f3ef56bc6f53c53894cdbbc84
sio:SIO_000628
miriam-gene:5243
,
lld:C0023448
;
a
sio:SIO_001122
.
}
dgn-np:NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_provenance
{
dgn-np:NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_assertion
dcterms:description
"[In conclusion, the results of the present study provide evidence that C3435T MDR1 polymorphism may involve both the susceptibility to and the clinical outcome of childhood ALL. Carriers of the TT genotype are more at risk of developing ALL than other indi]. 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:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:13+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}