@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP70067.RAotQITXp8LrJ9NbJvx7PXk0sFq-7fbKTmq8eHb1B3rQc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP70067.RAotQITXp8LrJ9NbJvx7PXk0sFq-7fbKTmq8eHb1B3rQc130_head
{
this:
np:hasAssertion
dgn-np:NP70067.RAotQITXp8LrJ9NbJvx7PXk0sFq-7fbKTmq8eHb1B3rQc130_assertion
;
np:hasProvenance
dgn-np:NP70067.RAotQITXp8LrJ9NbJvx7PXk0sFq-7fbKTmq8eHb1B3rQc130_provenance
;
np:hasPublicationInfo
dgn-np:NP70067.RAotQITXp8LrJ9NbJvx7PXk0sFq-7fbKTmq8eHb1B3rQc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP70067.RAotQITXp8LrJ9NbJvx7PXk0sFq-7fbKTmq8eHb1B3rQc130_assertion
a
np:Assertion
.
dgn-np:NP70067.RAotQITXp8LrJ9NbJvx7PXk0sFq-7fbKTmq8eHb1B3rQc130_provenance
a
np:Provenance
.
dgn-np:NP70067.RAotQITXp8LrJ9NbJvx7PXk0sFq-7fbKTmq8eHb1B3rQc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP70067.RAotQITXp8LrJ9NbJvx7PXk0sFq-7fbKTmq8eHb1B3rQc130_assertion
{
miriam-gene:4548
a
ncit:C16612
.
lld:C0024299
a
ncit:C7057
.
dgn-gda:DGNaee73419000d50ba0a949f2eacb80838
sio:SIO_000628
miriam-gene:4548
,
lld:C0024299
;
a
sio:SIO_001122
.
}
dgn-np:NP70067.RAotQITXp8LrJ9NbJvx7PXk0sFq-7fbKTmq8eHb1B3rQc130_provenance
{
dgn-np:NP70067.RAotQITXp8LrJ9NbJvx7PXk0sFq-7fbKTmq8eHb1B3rQc130_assertion
dcterms:description
"[Unconditional logistic regression analyses revealed a higher susceptibility with the MTHFR677 CC and the MTHFR1298 AA genotypes when those harboring at least one variant allele in either polymorphism of MTHFR were defined as the reference. For the MS poly]. 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:11342450
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP70067.RAotQITXp8LrJ9NbJvx7PXk0sFq-7fbKTmq8eHb1B3rQc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:20+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}