@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP921354.RAfj-PYn0tRcQ_ZqhkHVagodKJ-iNnFcYfYgd-pQ-QZLE
> .
@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:NP921354.RAfj-PYn0tRcQ_ZqhkHVagodKJ-iNnFcYfYgd-pQ-QZLE130_head
{
this:
np:hasAssertion
dgn-np:NP921354.RAfj-PYn0tRcQ_ZqhkHVagodKJ-iNnFcYfYgd-pQ-QZLE130_assertion
;
np:hasProvenance
dgn-np:NP921354.RAfj-PYn0tRcQ_ZqhkHVagodKJ-iNnFcYfYgd-pQ-QZLE130_provenance
;
np:hasPublicationInfo
dgn-np:NP921354.RAfj-PYn0tRcQ_ZqhkHVagodKJ-iNnFcYfYgd-pQ-QZLE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP921354.RAfj-PYn0tRcQ_ZqhkHVagodKJ-iNnFcYfYgd-pQ-QZLE130_assertion
a
np:Assertion
.
dgn-np:NP921354.RAfj-PYn0tRcQ_ZqhkHVagodKJ-iNnFcYfYgd-pQ-QZLE130_provenance
a
np:Provenance
.
dgn-np:NP921354.RAfj-PYn0tRcQ_ZqhkHVagodKJ-iNnFcYfYgd-pQ-QZLE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP921354.RAfj-PYn0tRcQ_ZqhkHVagodKJ-iNnFcYfYgd-pQ-QZLE130_assertion
{
miriam-gene:1565
a
ncit:C16612
.
lld:C0007130
a
ncit:C7057
.
dgn-gda:DGNfc588546c2e4179054f0457d31fa3896
sio:SIO_000628
miriam-gene:1565
,
lld:C0007130
;
a
sio:SIO_001121
.
}
dgn-np:NP921354.RAfj-PYn0tRcQ_ZqhkHVagodKJ-iNnFcYfYgd-pQ-QZLE130_provenance
{
dgn-np:NP921354.RAfj-PYn0tRcQ_ZqhkHVagodKJ-iNnFcYfYgd-pQ-QZLE130_assertion
dcterms:description
"[Relative to subjects with an inactivating allele, those with an additional copy of the CYP2D6 gene and no inactivating alleles may be at increased risk of lung cancer, particularly for adenocarcinoma (OR = 3.61, 95% CI 1.08-11.7 for African-Americans and OR = 2.20, 95% CI 0.69-6.0 for Caucasians).]. 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:9214604
;
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:NP921354.RAfj-PYn0tRcQ_ZqhkHVagodKJ-iNnFcYfYgd-pQ-QZLE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:25+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" .
}