@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP186819.RAONF9F_cnH771y8VHxyHt1LFx8bTYtsg8y7pjw6tYhhI
> .
@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:NP186819.RAONF9F_cnH771y8VHxyHt1LFx8bTYtsg8y7pjw6tYhhI130_head
{
this:
np:hasAssertion
dgn-np:NP186819.RAONF9F_cnH771y8VHxyHt1LFx8bTYtsg8y7pjw6tYhhI130_assertion
;
np:hasProvenance
dgn-np:NP186819.RAONF9F_cnH771y8VHxyHt1LFx8bTYtsg8y7pjw6tYhhI130_provenance
;
np:hasPublicationInfo
dgn-np:NP186819.RAONF9F_cnH771y8VHxyHt1LFx8bTYtsg8y7pjw6tYhhI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP186819.RAONF9F_cnH771y8VHxyHt1LFx8bTYtsg8y7pjw6tYhhI130_assertion
a
np:Assertion
.
dgn-np:NP186819.RAONF9F_cnH771y8VHxyHt1LFx8bTYtsg8y7pjw6tYhhI130_provenance
a
np:Provenance
.
dgn-np:NP186819.RAONF9F_cnH771y8VHxyHt1LFx8bTYtsg8y7pjw6tYhhI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP186819.RAONF9F_cnH771y8VHxyHt1LFx8bTYtsg8y7pjw6tYhhI130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0027794
a
ncit:C7057
.
dgn-gda:DGNa68f78c5c78ebdef5ef07c03c9e33ace
sio:SIO_000628
miriam-gene:4524
,
lld:C0027794
;
a
sio:SIO_001122
.
}
dgn-np:NP186819.RAONF9F_cnH771y8VHxyHt1LFx8bTYtsg8y7pjw6tYhhI130_provenance
{
dgn-np:NP186819.RAONF9F_cnH771y8VHxyHt1LFx8bTYtsg8y7pjw6tYhhI130_assertion
dcterms:description
"[The MTHFR 677TT genotype is considered to be a definite risk factor for development of NTDs. It is the TT genotype status of the developing embryo, rather than the TT genotype status of its mother, that is the critical genetic determinant of MTHFR-related]. 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:20887110
;
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:NP186819.RAONF9F_cnH771y8VHxyHt1LFx8bTYtsg8y7pjw6tYhhI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:11+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" .
}