@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M
> .
@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:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_head
{
this:
np:hasAssertion
dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_assertion
;
np:hasProvenance
dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_provenance
;
np:hasPublicationInfo
dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_assertion
a
np:Assertion
.
dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_provenance
a
np:Provenance
.
dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0747845
a
ncit:C7057
.
dgn-gda:DGNbcb900b505bcfb20e61cd93abe6f37e3
sio:SIO_000628
miriam-gene:4524
,
lld:C0747845
;
a
sio:SIO_001122
.
}
dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_provenance
{
dgn-np:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_assertion
dcterms:description
"[The methylenetetrahydrofolate reductase (MTHFR) gene C677T and A1298C polymorphisms are commonly associated with defects in folate dependent homocysteine metabolism and have been implicated as risk factors for recurrent embryo loss in early pregnancy.]. 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:11938441
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP351042.RAihmrXwmryeKhdNP5m1Jy916B45KtYaY8Q3xibQvgc4M130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:24+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" .
}