@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP84291.RAPAK-fYvqBKXao6A3u2Z2I3du3chGMgcPzYI8Cp3ubgw
> .
@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:NP84291.RAPAK-fYvqBKXao6A3u2Z2I3du3chGMgcPzYI8Cp3ubgw130_head
{
this:
np:hasAssertion
dgn-np:NP84291.RAPAK-fYvqBKXao6A3u2Z2I3du3chGMgcPzYI8Cp3ubgw130_assertion
;
np:hasProvenance
dgn-np:NP84291.RAPAK-fYvqBKXao6A3u2Z2I3du3chGMgcPzYI8Cp3ubgw130_provenance
;
np:hasPublicationInfo
dgn-np:NP84291.RAPAK-fYvqBKXao6A3u2Z2I3du3chGMgcPzYI8Cp3ubgw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP84291.RAPAK-fYvqBKXao6A3u2Z2I3du3chGMgcPzYI8Cp3ubgw130_assertion
a
np:Assertion
.
dgn-np:NP84291.RAPAK-fYvqBKXao6A3u2Z2I3du3chGMgcPzYI8Cp3ubgw130_provenance
a
np:Provenance
.
dgn-np:NP84291.RAPAK-fYvqBKXao6A3u2Z2I3du3chGMgcPzYI8Cp3ubgw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP84291.RAPAK-fYvqBKXao6A3u2Z2I3du3chGMgcPzYI8Cp3ubgw130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0000786
a
ncit:C7057
.
dgn-gda:DGN4dbbf04cee2d39236bbc326ab6142e94
sio:SIO_000628
miriam-gene:4524
,
lld:C0000786
;
a
sio:SIO_001122
.
}
dgn-np:NP84291.RAPAK-fYvqBKXao6A3u2Z2I3du3chGMgcPzYI8Cp3ubgw130_provenance
{
dgn-np:NP84291.RAPAK-fYvqBKXao6A3u2Z2I3du3chGMgcPzYI8Cp3ubgw130_assertion
dcterms:description
"[The subject of this study is analysis of genotypes and haplotypes of C677T and A1298C polymorphic variants of MTHFR genes in the groups of spontaneous abortions with the normal karyotype and newborns in the Tomsk population.]. 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:16808252
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP84291.RAPAK-fYvqBKXao6A3u2Z2I3du3chGMgcPzYI8Cp3ubgw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:41+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" .
}