@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8
> .
@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:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_head
{
this:
np:hasAssertion
dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_assertion
;
np:hasProvenance
dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_provenance
;
np:hasPublicationInfo
dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_assertion
a
np:Assertion
.
dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_provenance
a
np:Provenance
.
dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_assertion
{
miriam-gene:4683
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGNab47c5a1be09f30f5c6f948d008ca70b
sio:SIO_000628
miriam-gene:4683
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_provenance
{
dgn-np:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_assertion
dcterms:description
"[Our results show that the genetic variation in XRCC1, XRCC3 and NBS1 influence lung cancer susceptibility among women, and that combinations of risk alleles in the two HR genes can enhance the effects.]. 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:17034901
;
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:NP559368.RAN3Mi7Fdl2mlHbYuuF1882NNpuY2BwLSYCFxd6eNcvc8130_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" .
}