@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP534981.RAfUAW012ifpYrzPzdv6FpzCv1CQASRQvXaZU5i12evMg
> .
@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:NP534981.RAfUAW012ifpYrzPzdv6FpzCv1CQASRQvXaZU5i12evMg130_head
{
this:
np:hasAssertion
dgn-np:NP534981.RAfUAW012ifpYrzPzdv6FpzCv1CQASRQvXaZU5i12evMg130_assertion
;
np:hasProvenance
dgn-np:NP534981.RAfUAW012ifpYrzPzdv6FpzCv1CQASRQvXaZU5i12evMg130_provenance
;
np:hasPublicationInfo
dgn-np:NP534981.RAfUAW012ifpYrzPzdv6FpzCv1CQASRQvXaZU5i12evMg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP534981.RAfUAW012ifpYrzPzdv6FpzCv1CQASRQvXaZU5i12evMg130_assertion
a
np:Assertion
.
dgn-np:NP534981.RAfUAW012ifpYrzPzdv6FpzCv1CQASRQvXaZU5i12evMg130_provenance
a
np:Provenance
.
dgn-np:NP534981.RAfUAW012ifpYrzPzdv6FpzCv1CQASRQvXaZU5i12evMg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP534981.RAfUAW012ifpYrzPzdv6FpzCv1CQASRQvXaZU5i12evMg130_assertion
{
miriam-gene:196
a
ncit:C16612
.
lld:C1519689
a
ncit:C7057
.
dgn-gda:DGN7ba4f334b8e4e555f46fd3a20d6516e7
sio:SIO_000628
miriam-gene:196
,
lld:C1519689
;
a
sio:SIO_001121
.
}
dgn-np:NP534981.RAfUAW012ifpYrzPzdv6FpzCv1CQASRQvXaZU5i12evMg130_provenance
{
dgn-np:NP534981.RAfUAW012ifpYrzPzdv6FpzCv1CQASRQvXaZU5i12evMg130_assertion
dcterms:description
"[It is most likely that the correlation between genetic differences in human or murine CYP1A1 inducibility by polycyclic hydrocarbons or TCDD and increased risk of cancer will be explained by differences in the AHR gene, leading to enhanced tumor promotion (rather than in the CYP1A1 structural gene).]. 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:8395783
;
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:NP534981.RAfUAW012ifpYrzPzdv6FpzCv1CQASRQvXaZU5i12evMg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:23+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" .
}