@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP589737.RA39GfR9PwavIqfj4QaOklA3QSoPNJvgJNK91HVKb7UzA
> .
@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:NP589737.RA39GfR9PwavIqfj4QaOklA3QSoPNJvgJNK91HVKb7UzA130_head
{
this:
np:hasAssertion
dgn-np:NP589737.RA39GfR9PwavIqfj4QaOklA3QSoPNJvgJNK91HVKb7UzA130_assertion
;
np:hasProvenance
dgn-np:NP589737.RA39GfR9PwavIqfj4QaOklA3QSoPNJvgJNK91HVKb7UzA130_provenance
;
np:hasPublicationInfo
dgn-np:NP589737.RA39GfR9PwavIqfj4QaOklA3QSoPNJvgJNK91HVKb7UzA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP589737.RA39GfR9PwavIqfj4QaOklA3QSoPNJvgJNK91HVKb7UzA130_assertion
a
np:Assertion
.
dgn-np:NP589737.RA39GfR9PwavIqfj4QaOklA3QSoPNJvgJNK91HVKb7UzA130_provenance
a
np:Provenance
.
dgn-np:NP589737.RA39GfR9PwavIqfj4QaOklA3QSoPNJvgJNK91HVKb7UzA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP589737.RA39GfR9PwavIqfj4QaOklA3QSoPNJvgJNK91HVKb7UzA130_assertion
{
miriam-gene:1559
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNae4b97492c81fe47d396e0f8b02e55a6
sio:SIO_000628
miriam-gene:1559
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP589737.RA39GfR9PwavIqfj4QaOklA3QSoPNJvgJNK91HVKb7UzA130_provenance
{
dgn-np:NP589737.RA39GfR9PwavIqfj4QaOklA3QSoPNJvgJNK91HVKb7UzA130_assertion
dcterms:description
"[Recently, large studies on the association between genetic variation in CYP1B1 and CYP2C9 and risk of disease with considerable statistical power rebutted the hypotheses that these genetic variants affect risk of tobacco-related cancer, female cancer, chronic obstructive pulmonary disease and ischemic vascular disease.]. 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:22272893
;
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:NP589737.RA39GfR9PwavIqfj4QaOklA3QSoPNJvgJNK91HVKb7UzA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:55+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" .
}