@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP130831.RAXt_-hGMU-_hkfAe2tgB5_qWgtQy65F8jzFgTAqqbd_s
> .
@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/v3.0.0/void/
> .
dgn-np:NP130831.RAXt_-hGMU-_hkfAe2tgB5_qWgtQy65F8jzFgTAqqbd_s130_head
{
this:
np:hasAssertion
dgn-np:NP130831.RAXt_-hGMU-_hkfAe2tgB5_qWgtQy65F8jzFgTAqqbd_s130_assertion
;
np:hasProvenance
dgn-np:NP130831.RAXt_-hGMU-_hkfAe2tgB5_qWgtQy65F8jzFgTAqqbd_s130_provenance
;
np:hasPublicationInfo
dgn-np:NP130831.RAXt_-hGMU-_hkfAe2tgB5_qWgtQy65F8jzFgTAqqbd_s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP130831.RAXt_-hGMU-_hkfAe2tgB5_qWgtQy65F8jzFgTAqqbd_s130_assertion
a
np:Assertion
.
dgn-np:NP130831.RAXt_-hGMU-_hkfAe2tgB5_qWgtQy65F8jzFgTAqqbd_s130_provenance
a
np:Provenance
.
dgn-np:NP130831.RAXt_-hGMU-_hkfAe2tgB5_qWgtQy65F8jzFgTAqqbd_s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP130831.RAXt_-hGMU-_hkfAe2tgB5_qWgtQy65F8jzFgTAqqbd_s130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0012628
a
ncit:C7057
.
dgn-gda:DGN6d0839ec34c9cc5d0db92f5fa0b86c5c
sio:SIO_000628
miriam-gene:4524
,
lld:C0012628
;
a
sio:SIO_001122
.
}
dgn-np:NP130831.RAXt_-hGMU-_hkfAe2tgB5_qWgtQy65F8jzFgTAqqbd_s130_provenance
{
dgn-np:NP130831.RAXt_-hGMU-_hkfAe2tgB5_qWgtQy65F8jzFgTAqqbd_s130_assertion
dcterms:description
"[With the present study we can show for the first time that the embryonal MTHFR 677TT genotype is significantly associated with the development of structural congenital heart malformations during 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:11470464
;
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:NP130831.RAXt_-hGMU-_hkfAe2tgB5_qWgtQy65F8jzFgTAqqbd_s130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:53+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}