@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP559788.RA4hveEXiLdIfz2YXxWg6cqX-QDr37bunQOGXMhyoAQYk
> .
@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:NP559788.RA4hveEXiLdIfz2YXxWg6cqX-QDr37bunQOGXMhyoAQYk130_head
{
this:
np:hasAssertion
dgn-np:NP559788.RA4hveEXiLdIfz2YXxWg6cqX-QDr37bunQOGXMhyoAQYk130_assertion
;
np:hasProvenance
dgn-np:NP559788.RA4hveEXiLdIfz2YXxWg6cqX-QDr37bunQOGXMhyoAQYk130_provenance
;
np:hasPublicationInfo
dgn-np:NP559788.RA4hveEXiLdIfz2YXxWg6cqX-QDr37bunQOGXMhyoAQYk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP559788.RA4hveEXiLdIfz2YXxWg6cqX-QDr37bunQOGXMhyoAQYk130_assertion
a
np:Assertion
.
dgn-np:NP559788.RA4hveEXiLdIfz2YXxWg6cqX-QDr37bunQOGXMhyoAQYk130_provenance
a
np:Provenance
.
dgn-np:NP559788.RA4hveEXiLdIfz2YXxWg6cqX-QDr37bunQOGXMhyoAQYk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP559788.RA4hveEXiLdIfz2YXxWg6cqX-QDr37bunQOGXMhyoAQYk130_assertion
{
miriam-gene:7376
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN758075d74d3bab52baed9b4e2b848800
sio:SIO_000628
miriam-gene:7376
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP559788.RA4hveEXiLdIfz2YXxWg6cqX-QDr37bunQOGXMhyoAQYk130_provenance
{
dgn-np:NP559788.RA4hveEXiLdIfz2YXxWg6cqX-QDr37bunQOGXMhyoAQYk130_assertion
dcterms:description
"[Inter individual variation in lung cancer susceptibility may be modulated in part through genetic polymorphisms in the DNA repair genes, especially the genes involved in the Base Excision Repair (BER) and nucleotide excision repair (NER) pathway.]. 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:17952468
;
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:NP559788.RA4hveEXiLdIfz2YXxWg6cqX-QDr37bunQOGXMhyoAQYk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:37+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" .
}