@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP563722.RAXH9PQwcJKtXd4522_fsCJpmPWJIKPYYmMpMB9DpB2M0
> .
@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:NP563722.RAXH9PQwcJKtXd4522_fsCJpmPWJIKPYYmMpMB9DpB2M0130_head
{
this:
np:hasAssertion
dgn-np:NP563722.RAXH9PQwcJKtXd4522_fsCJpmPWJIKPYYmMpMB9DpB2M0130_assertion
;
np:hasProvenance
dgn-np:NP563722.RAXH9PQwcJKtXd4522_fsCJpmPWJIKPYYmMpMB9DpB2M0130_provenance
;
np:hasPublicationInfo
dgn-np:NP563722.RAXH9PQwcJKtXd4522_fsCJpmPWJIKPYYmMpMB9DpB2M0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP563722.RAXH9PQwcJKtXd4522_fsCJpmPWJIKPYYmMpMB9DpB2M0130_assertion
a
np:Assertion
.
dgn-np:NP563722.RAXH9PQwcJKtXd4522_fsCJpmPWJIKPYYmMpMB9DpB2M0130_provenance
a
np:Provenance
.
dgn-np:NP563722.RAXH9PQwcJKtXd4522_fsCJpmPWJIKPYYmMpMB9DpB2M0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP563722.RAXH9PQwcJKtXd4522_fsCJpmPWJIKPYYmMpMB9DpB2M0130_assertion
{
miriam-gene:2052
a
ncit:C16612
.
lld:C1704273
a
ncit:C7057
.
dgn-gda:DGN5e8a0320f768bc763b9bee0401afe112
sio:SIO_000628
miriam-gene:2052
,
lld:C1704273
;
a
sio:SIO_001121
.
}
dgn-np:NP563722.RAXH9PQwcJKtXd4522_fsCJpmPWJIKPYYmMpMB9DpB2M0130_provenance
{
dgn-np:NP563722.RAXH9PQwcJKtXd4522_fsCJpmPWJIKPYYmMpMB9DpB2M0130_assertion
dcterms:description
"[In an analysis controlling only for the matching variables, we found little or no association between adenoma and mEH genotypes defined by polymorphisms at either codon 113 and 139 or mEH activity predicted by both polymorphisms.]. 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:11289100
;
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:NP563722.RAXH9PQwcJKtXd4522_fsCJpmPWJIKPYYmMpMB9DpB2M0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}