@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP282803.RAhAthouMRqL8D0OxtzGC9XOAMvhZMBe5sECGki0ZJb0Q
> .
@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:NP282803.RAhAthouMRqL8D0OxtzGC9XOAMvhZMBe5sECGki0ZJb0Q130_head
{
this:
np:hasAssertion
dgn-np:NP282803.RAhAthouMRqL8D0OxtzGC9XOAMvhZMBe5sECGki0ZJb0Q130_assertion
;
np:hasProvenance
dgn-np:NP282803.RAhAthouMRqL8D0OxtzGC9XOAMvhZMBe5sECGki0ZJb0Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP282803.RAhAthouMRqL8D0OxtzGC9XOAMvhZMBe5sECGki0ZJb0Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP282803.RAhAthouMRqL8D0OxtzGC9XOAMvhZMBe5sECGki0ZJb0Q130_assertion
a
np:Assertion
.
dgn-np:NP282803.RAhAthouMRqL8D0OxtzGC9XOAMvhZMBe5sECGki0ZJb0Q130_provenance
a
np:Provenance
.
dgn-np:NP282803.RAhAthouMRqL8D0OxtzGC9XOAMvhZMBe5sECGki0ZJb0Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP282803.RAhAthouMRqL8D0OxtzGC9XOAMvhZMBe5sECGki0ZJb0Q130_assertion
{
miriam-gene:10
a
ncit:C16612
.
lld:C1827820
a
ncit:C7057
.
dgn-gda:DGN73233c907f34c8065fe0df2a934483ce
sio:SIO_000628
miriam-gene:10
,
lld:C1827820
;
a
sio:SIO_001121
.
}
dgn-np:NP282803.RAhAthouMRqL8D0OxtzGC9XOAMvhZMBe5sECGki0ZJb0Q130_provenance
{
dgn-np:NP282803.RAhAthouMRqL8D0OxtzGC9XOAMvhZMBe5sECGki0ZJb0Q130_assertion
dcterms:description
"[The MTHFR codon 222 variant allele was associated with high CTGs in smokers, the MTR codon 919 variant allele with high CTAs in older smokers and the NAT2 fast acetylator genotype with high CTGs in older subjects.]. 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:21097530
;
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:NP282803.RAhAthouMRqL8D0OxtzGC9XOAMvhZMBe5sECGki0ZJb0Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:39+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" .
}