@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP70783.RAC0fxpv-rIQlD-p-ndJ3Swgye-3DpuQ1U5dlgQhXijnc
> .
@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:NP70783.RAC0fxpv-rIQlD-p-ndJ3Swgye-3DpuQ1U5dlgQhXijnc130_head
{
this:
np:hasAssertion
dgn-np:NP70783.RAC0fxpv-rIQlD-p-ndJ3Swgye-3DpuQ1U5dlgQhXijnc130_assertion
;
np:hasProvenance
dgn-np:NP70783.RAC0fxpv-rIQlD-p-ndJ3Swgye-3DpuQ1U5dlgQhXijnc130_provenance
;
np:hasPublicationInfo
dgn-np:NP70783.RAC0fxpv-rIQlD-p-ndJ3Swgye-3DpuQ1U5dlgQhXijnc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP70783.RAC0fxpv-rIQlD-p-ndJ3Swgye-3DpuQ1U5dlgQhXijnc130_assertion
a
np:Assertion
.
dgn-np:NP70783.RAC0fxpv-rIQlD-p-ndJ3Swgye-3DpuQ1U5dlgQhXijnc130_provenance
a
np:Provenance
.
dgn-np:NP70783.RAC0fxpv-rIQlD-p-ndJ3Swgye-3DpuQ1U5dlgQhXijnc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP70783.RAC0fxpv-rIQlD-p-ndJ3Swgye-3DpuQ1U5dlgQhXijnc130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0034089
a
ncit:C7057
.
dgn-gda:DGN833781a3866f95e0006067293a55ea22
sio:SIO_000628
miriam-gene:4524
,
lld:C0034089
;
a
sio:SIO_001122
.
}
dgn-np:NP70783.RAC0fxpv-rIQlD-p-ndJ3Swgye-3DpuQ1U5dlgQhXijnc130_provenance
{
dgn-np:NP70783.RAC0fxpv-rIQlD-p-ndJ3Swgye-3DpuQ1U5dlgQhXijnc130_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:NP70783.RAC0fxpv-rIQlD-p-ndJ3Swgye-3DpuQ1U5dlgQhXijnc130_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" .
}