@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP566052.RAW-7huzC8jOvAxVorRBShs7K30iXI_3YWoTEpXP6-dwY
> .
@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:NP566052.RAW-7huzC8jOvAxVorRBShs7K30iXI_3YWoTEpXP6-dwY130_head
{
this:
np:hasAssertion
dgn-np:NP566052.RAW-7huzC8jOvAxVorRBShs7K30iXI_3YWoTEpXP6-dwY130_assertion
;
np:hasProvenance
dgn-np:NP566052.RAW-7huzC8jOvAxVorRBShs7K30iXI_3YWoTEpXP6-dwY130_provenance
;
np:hasPublicationInfo
dgn-np:NP566052.RAW-7huzC8jOvAxVorRBShs7K30iXI_3YWoTEpXP6-dwY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP566052.RAW-7huzC8jOvAxVorRBShs7K30iXI_3YWoTEpXP6-dwY130_assertion
a
np:Assertion
.
dgn-np:NP566052.RAW-7huzC8jOvAxVorRBShs7K30iXI_3YWoTEpXP6-dwY130_provenance
a
np:Provenance
.
dgn-np:NP566052.RAW-7huzC8jOvAxVorRBShs7K30iXI_3YWoTEpXP6-dwY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP566052.RAW-7huzC8jOvAxVorRBShs7K30iXI_3YWoTEpXP6-dwY130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0747845
a
ncit:C7057
.
dgn-gda:DGN3983a532dd21684a56b037e02dabe825
sio:SIO_000628
miriam-gene:4524
,
lld:C0747845
;
a
sio:SIO_001121
.
}
dgn-np:NP566052.RAW-7huzC8jOvAxVorRBShs7K30iXI_3YWoTEpXP6-dwY130_provenance
{
dgn-np:NP566052.RAW-7huzC8jOvAxVorRBShs7K30iXI_3YWoTEpXP6-dwY130_assertion
dcterms:description
"[Because of MTHFR's involvement with folate metabolism and evidence that maternal use of a multivitamin with folic acid in early pregnancy reduces risk for cleft lip with or without cleft palate (CLP), we hypothesized that infants homozygous for the C677T genotype would be at increased risk for CLP because of lower MTHFR enzymatic activity.]. 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:9843036
;
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:NP566052.RAW-7huzC8jOvAxVorRBShs7K30iXI_3YWoTEpXP6-dwY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:41+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" .
}