@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP518744.RAtcEJMYFG1hPXUpHNRW7l4TyINIqYqdFzeqoB6Xxd_gk
> .
@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:NP518744.RAtcEJMYFG1hPXUpHNRW7l4TyINIqYqdFzeqoB6Xxd_gk130_head
{
this:
np:hasAssertion
dgn-np:NP518744.RAtcEJMYFG1hPXUpHNRW7l4TyINIqYqdFzeqoB6Xxd_gk130_assertion
;
np:hasProvenance
dgn-np:NP518744.RAtcEJMYFG1hPXUpHNRW7l4TyINIqYqdFzeqoB6Xxd_gk130_provenance
;
np:hasPublicationInfo
dgn-np:NP518744.RAtcEJMYFG1hPXUpHNRW7l4TyINIqYqdFzeqoB6Xxd_gk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP518744.RAtcEJMYFG1hPXUpHNRW7l4TyINIqYqdFzeqoB6Xxd_gk130_assertion
a
np:Assertion
.
dgn-np:NP518744.RAtcEJMYFG1hPXUpHNRW7l4TyINIqYqdFzeqoB6Xxd_gk130_provenance
a
np:Provenance
.
dgn-np:NP518744.RAtcEJMYFG1hPXUpHNRW7l4TyINIqYqdFzeqoB6Xxd_gk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP518744.RAtcEJMYFG1hPXUpHNRW7l4TyINIqYqdFzeqoB6Xxd_gk130_assertion
{
miriam-gene:80199
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGN3d325f6bbdda7364c67703fe4eecca54
sio:SIO_000628
miriam-gene:80199
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP518744.RAtcEJMYFG1hPXUpHNRW7l4TyINIqYqdFzeqoB6Xxd_gk130_provenance
{
dgn-np:NP518744.RAtcEJMYFG1hPXUpHNRW7l4TyINIqYqdFzeqoB6Xxd_gk130_assertion
dcterms:description
"[The presence of both trisomy 21 and postclosure NTD in the same child supports the need for an extended periconceptional period of maternal folate supplementation to achieve greater preventive effects for both NTD and trisomy 21.]. 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:11568918
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP518744.RAtcEJMYFG1hPXUpHNRW7l4TyINIqYqdFzeqoB6Xxd_gk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:09+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" .
}