@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP560921.RARTLgg1-4TKBcgdXtviUCU58Ouao4BTrar87p5gNWE1A
> .
@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:NP560921.RARTLgg1-4TKBcgdXtviUCU58Ouao4BTrar87p5gNWE1A130_head
{
this:
np:hasAssertion
dgn-np:NP560921.RARTLgg1-4TKBcgdXtviUCU58Ouao4BTrar87p5gNWE1A130_assertion
;
np:hasProvenance
dgn-np:NP560921.RARTLgg1-4TKBcgdXtviUCU58Ouao4BTrar87p5gNWE1A130_provenance
;
np:hasPublicationInfo
dgn-np:NP560921.RARTLgg1-4TKBcgdXtviUCU58Ouao4BTrar87p5gNWE1A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP560921.RARTLgg1-4TKBcgdXtviUCU58Ouao4BTrar87p5gNWE1A130_assertion
a
np:Assertion
.
dgn-np:NP560921.RARTLgg1-4TKBcgdXtviUCU58Ouao4BTrar87p5gNWE1A130_provenance
a
np:Provenance
.
dgn-np:NP560921.RARTLgg1-4TKBcgdXtviUCU58Ouao4BTrar87p5gNWE1A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP560921.RARTLgg1-4TKBcgdXtviUCU58Ouao4BTrar87p5gNWE1A130_assertion
{
miriam-gene:4709
a
ncit:C16612
.
lld:C0032962
a
ncit:C7057
.
dgn-gda:DGN13326182e92ff638af9fc658cefa7c44
sio:SIO_000628
miriam-gene:4709
,
lld:C0032962
;
a
sio:SIO_001121
.
}
dgn-np:NP560921.RARTLgg1-4TKBcgdXtviUCU58Ouao4BTrar87p5gNWE1A130_provenance
{
dgn-np:NP560921.RARTLgg1-4TKBcgdXtviUCU58Ouao4BTrar87p5gNWE1A130_assertion
dcterms:description
"[Although tHcy seems to be physiologically low in this Spanish population and unrelated to folate and B12 nutritional status, C677T MTHFR genotype, and some pregnancy complications, we support the statement that appropriate folate concentration may be important throughout pregnancy to prevent abnormalities associated with altered status (e.g., neural tube defects).]. 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:21367581
;
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:NP560921.RARTLgg1-4TKBcgdXtviUCU58Ouao4BTrar87p5gNWE1A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}