@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP204208.RAtfZP3HNRgFskzcPz2tFE_zMXqtwwgDpUlS0cH6hK3yw
> .
@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:NP204208.RAtfZP3HNRgFskzcPz2tFE_zMXqtwwgDpUlS0cH6hK3yw130_head
{
this:
np:hasAssertion
dgn-np:NP204208.RAtfZP3HNRgFskzcPz2tFE_zMXqtwwgDpUlS0cH6hK3yw130_assertion
;
np:hasProvenance
dgn-np:NP204208.RAtfZP3HNRgFskzcPz2tFE_zMXqtwwgDpUlS0cH6hK3yw130_provenance
;
np:hasPublicationInfo
dgn-np:NP204208.RAtfZP3HNRgFskzcPz2tFE_zMXqtwwgDpUlS0cH6hK3yw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP204208.RAtfZP3HNRgFskzcPz2tFE_zMXqtwwgDpUlS0cH6hK3yw130_assertion
a
np:Assertion
.
dgn-np:NP204208.RAtfZP3HNRgFskzcPz2tFE_zMXqtwwgDpUlS0cH6hK3yw130_provenance
a
np:Provenance
.
dgn-np:NP204208.RAtfZP3HNRgFskzcPz2tFE_zMXqtwwgDpUlS0cH6hK3yw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP204208.RAtfZP3HNRgFskzcPz2tFE_zMXqtwwgDpUlS0cH6hK3yw130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0018798
a
ncit:C7057
.
dgn-gda:DGNce9654e40e7b6d113596b29b369dd39a
sio:SIO_000628
miriam-gene:4524
,
lld:C0018798
;
a
sio:SIO_001121
.
}
dgn-np:NP204208.RAtfZP3HNRgFskzcPz2tFE_zMXqtwwgDpUlS0cH6hK3yw130_provenance
{
dgn-np:NP204208.RAtfZP3HNRgFskzcPz2tFE_zMXqtwwgDpUlS0cH6hK3yw130_assertion
dcterms:description
"[This case-control study aimed to evaluate the effect of maternal C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase (MTHFR) as risk factors for the development of DS and congenital heart defects (CHD).]. 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:19725133
;
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:NP204208.RAtfZP3HNRgFskzcPz2tFE_zMXqtwwgDpUlS0cH6hK3yw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:52+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" .
}