@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP635591.RAL9qg9EdTUoE9tH_4Pzw9CCunhhS1OZdUEeU9LaWmRBE
> .
@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:NP635591.RAL9qg9EdTUoE9tH_4Pzw9CCunhhS1OZdUEeU9LaWmRBE130_head
{
this:
np:hasAssertion
dgn-np:NP635591.RAL9qg9EdTUoE9tH_4Pzw9CCunhhS1OZdUEeU9LaWmRBE130_assertion
;
np:hasProvenance
dgn-np:NP635591.RAL9qg9EdTUoE9tH_4Pzw9CCunhhS1OZdUEeU9LaWmRBE130_provenance
;
np:hasPublicationInfo
dgn-np:NP635591.RAL9qg9EdTUoE9tH_4Pzw9CCunhhS1OZdUEeU9LaWmRBE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP635591.RAL9qg9EdTUoE9tH_4Pzw9CCunhhS1OZdUEeU9LaWmRBE130_assertion
a
np:Assertion
.
dgn-np:NP635591.RAL9qg9EdTUoE9tH_4Pzw9CCunhhS1OZdUEeU9LaWmRBE130_provenance
a
np:Provenance
.
dgn-np:NP635591.RAL9qg9EdTUoE9tH_4Pzw9CCunhhS1OZdUEeU9LaWmRBE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP635591.RAL9qg9EdTUoE9tH_4Pzw9CCunhhS1OZdUEeU9LaWmRBE130_assertion
{
miriam-gene:1571
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGN64646c40a17ed06c22ba5cfb80581708
sio:SIO_000628
miriam-gene:1571
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP635591.RAL9qg9EdTUoE9tH_4Pzw9CCunhhS1OZdUEeU9LaWmRBE130_provenance
{
dgn-np:NP635591.RAL9qg9EdTUoE9tH_4Pzw9CCunhhS1OZdUEeU9LaWmRBE130_assertion
dcterms:description
"[Part of the reason for conflicting evidence regarding genotype effect on phenotype may be due to the wide variety of exposures such as ethanol or dietary factors and physiological factors including body weight or diabetes that modulate CYP2E1 expression.]. 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:20183527
;
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:NP635591.RAL9qg9EdTUoE9tH_4Pzw9CCunhhS1OZdUEeU9LaWmRBE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:23+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" .
}