@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP79761.RAYq7gv_rxNNVChMeDeiAEEwFi5zaVMLIym-Esm8TDShc
> .
@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 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:NP79761.RAYq7gv_rxNNVChMeDeiAEEwFi5zaVMLIym-Esm8TDShc130_head
{
this:
np:hasAssertion
dgn-np:NP79761.RAYq7gv_rxNNVChMeDeiAEEwFi5zaVMLIym-Esm8TDShc130_assertion
;
np:hasProvenance
dgn-np:NP79761.RAYq7gv_rxNNVChMeDeiAEEwFi5zaVMLIym-Esm8TDShc130_provenance
;
np:hasPublicationInfo
dgn-np:NP79761.RAYq7gv_rxNNVChMeDeiAEEwFi5zaVMLIym-Esm8TDShc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP79761.RAYq7gv_rxNNVChMeDeiAEEwFi5zaVMLIym-Esm8TDShc130_assertion
a
np:Assertion
.
dgn-np:NP79761.RAYq7gv_rxNNVChMeDeiAEEwFi5zaVMLIym-Esm8TDShc130_provenance
a
np:Provenance
.
dgn-np:NP79761.RAYq7gv_rxNNVChMeDeiAEEwFi5zaVMLIym-Esm8TDShc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP79761.RAYq7gv_rxNNVChMeDeiAEEwFi5zaVMLIym-Esm8TDShc130_assertion
{
miriam-gene:7515
a
ncit:C16612
.
lld:C1961102
a
ncit:C7057
.
dgn-gda:DGNb3270914b5923a388c2e7a2039e67fe6
sio:SIO_000628
miriam-gene:7515
,
lld:C1961102
;
a
sio:SIO_001122
.
}
dgn-np:NP79761.RAYq7gv_rxNNVChMeDeiAEEwFi5zaVMLIym-Esm8TDShc130_provenance
{
dgn-np:NP79761.RAYq7gv_rxNNVChMeDeiAEEwFi5zaVMLIym-Esm8TDShc130_assertion
dc:description
"[We used polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP), to analyze XPD Asp312Asn, XPD Lys751Gln, XRCC1 Arg194Trp, and XRCC1 Arg399Gln polymorphisms in 70 patients with childhood ALL and in 75 disease-free controls, who were of a similar age.]. 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:19101034
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP79761.RAYq7gv_rxNNVChMeDeiAEEwFi5zaVMLIym-Esm8TDShc130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:39+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}