@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP871047.RAi6WxxLNO2KhaI7O1MlCSMIB5mSwAIZRhOZMM2R_n37Y
> .
@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:NP871047.RAi6WxxLNO2KhaI7O1MlCSMIB5mSwAIZRhOZMM2R_n37Y130_head
{
this:
np:hasAssertion
dgn-np:NP871047.RAi6WxxLNO2KhaI7O1MlCSMIB5mSwAIZRhOZMM2R_n37Y130_assertion
;
np:hasProvenance
dgn-np:NP871047.RAi6WxxLNO2KhaI7O1MlCSMIB5mSwAIZRhOZMM2R_n37Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP871047.RAi6WxxLNO2KhaI7O1MlCSMIB5mSwAIZRhOZMM2R_n37Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP871047.RAi6WxxLNO2KhaI7O1MlCSMIB5mSwAIZRhOZMM2R_n37Y130_assertion
a
np:Assertion
.
dgn-np:NP871047.RAi6WxxLNO2KhaI7O1MlCSMIB5mSwAIZRhOZMM2R_n37Y130_provenance
a
np:Provenance
.
dgn-np:NP871047.RAi6WxxLNO2KhaI7O1MlCSMIB5mSwAIZRhOZMM2R_n37Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP871047.RAi6WxxLNO2KhaI7O1MlCSMIB5mSwAIZRhOZMM2R_n37Y130_assertion
{
miriam-gene:7515
a
ncit:C16612
.
lld:C0549473
a
ncit:C7057
.
dgn-gda:DGN3454ec60e8829fd85e52793f1aa95e3e
sio:SIO_000628
miriam-gene:7515
,
lld:C0549473
;
a
sio:SIO_001121
.
}
dgn-np:NP871047.RAi6WxxLNO2KhaI7O1MlCSMIB5mSwAIZRhOZMM2R_n37Y130_provenance
{
dgn-np:NP871047.RAi6WxxLNO2KhaI7O1MlCSMIB5mSwAIZRhOZMM2R_n37Y130_assertion
dcterms:description
"[Our results do not reveal a significant involvement of XRCC1 Arg194Trp and Arg399Gln, OGG1 Ser326Cys, APEX1 Asp148Glu, MUTYH Gln335His and PARP1 Val762Ala polymorphisms on the individual susceptibility towards TC, mostly in agreement with the limited available evidence.]. 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:22922830
;
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:NP871047.RAi6WxxLNO2KhaI7O1MlCSMIB5mSwAIZRhOZMM2R_n37Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:52+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" .
}