@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP647328.RAWGaw6NMx_rj73nmpTOyU_Vtd0pIMnZEuZPhdc2h3W-U
> .
@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:NP647328.RAWGaw6NMx_rj73nmpTOyU_Vtd0pIMnZEuZPhdc2h3W-U130_head
{
this:
np:hasAssertion
dgn-np:NP647328.RAWGaw6NMx_rj73nmpTOyU_Vtd0pIMnZEuZPhdc2h3W-U130_assertion
;
np:hasProvenance
dgn-np:NP647328.RAWGaw6NMx_rj73nmpTOyU_Vtd0pIMnZEuZPhdc2h3W-U130_provenance
;
np:hasPublicationInfo
dgn-np:NP647328.RAWGaw6NMx_rj73nmpTOyU_Vtd0pIMnZEuZPhdc2h3W-U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP647328.RAWGaw6NMx_rj73nmpTOyU_Vtd0pIMnZEuZPhdc2h3W-U130_assertion
a
np:Assertion
.
dgn-np:NP647328.RAWGaw6NMx_rj73nmpTOyU_Vtd0pIMnZEuZPhdc2h3W-U130_provenance
a
np:Provenance
.
dgn-np:NP647328.RAWGaw6NMx_rj73nmpTOyU_Vtd0pIMnZEuZPhdc2h3W-U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP647328.RAWGaw6NMx_rj73nmpTOyU_Vtd0pIMnZEuZPhdc2h3W-U130_assertion
{
miriam-gene:142
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGN478e0bd7bd3fdcddb56322a9008fcdbd
sio:SIO_000628
miriam-gene:142
,
lld:C0023452
;
a
sio:SIO_001121
.
}
dgn-np:NP647328.RAWGaw6NMx_rj73nmpTOyU_Vtd0pIMnZEuZPhdc2h3W-U130_provenance
{
dgn-np:NP647328.RAWGaw6NMx_rj73nmpTOyU_Vtd0pIMnZEuZPhdc2h3W-U130_assertion
dcterms:description
"[Genetic polymorphisms in XRCC1 gene could, through alteration of protein structure, lead to defective functioning of DNA Polbeta, PARP and LIG3 enzymes resulting in defective DNA repair and increased risk of childhood acute lymphoblastic leukemia (ALL).]. 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:15596292
;
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:NP647328.RAWGaw6NMx_rj73nmpTOyU_Vtd0pIMnZEuZPhdc2h3W-U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:30+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" .
}