@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP210029.RA80nAJEqYdh0Qw0EuazTWvpi8gX4IQQ4jAOhPCyT4tlc
> .
@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:NP210029.RA80nAJEqYdh0Qw0EuazTWvpi8gX4IQQ4jAOhPCyT4tlc130_head
{
this:
np:hasAssertion
dgn-np:NP210029.RA80nAJEqYdh0Qw0EuazTWvpi8gX4IQQ4jAOhPCyT4tlc130_assertion
;
np:hasProvenance
dgn-np:NP210029.RA80nAJEqYdh0Qw0EuazTWvpi8gX4IQQ4jAOhPCyT4tlc130_provenance
;
np:hasPublicationInfo
dgn-np:NP210029.RA80nAJEqYdh0Qw0EuazTWvpi8gX4IQQ4jAOhPCyT4tlc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP210029.RA80nAJEqYdh0Qw0EuazTWvpi8gX4IQQ4jAOhPCyT4tlc130_assertion
a
np:Assertion
.
dgn-np:NP210029.RA80nAJEqYdh0Qw0EuazTWvpi8gX4IQQ4jAOhPCyT4tlc130_provenance
a
np:Provenance
.
dgn-np:NP210029.RA80nAJEqYdh0Qw0EuazTWvpi8gX4IQQ4jAOhPCyT4tlc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP210029.RA80nAJEqYdh0Qw0EuazTWvpi8gX4IQQ4jAOhPCyT4tlc130_assertion
{
miriam-gene:875
a
ncit:C16612
.
lld:C0080178
a
ncit:C7057
.
dgn-gda:DGN80319b5a60ef42265181947fb88a3d27
sio:SIO_000628
miriam-gene:875
,
lld:C0080178
;
a
sio:SIO_001121
.
}
dgn-np:NP210029.RA80nAJEqYdh0Qw0EuazTWvpi8gX4IQQ4jAOhPCyT4tlc130_provenance
{
dgn-np:NP210029.RA80nAJEqYdh0Qw0EuazTWvpi8gX4IQQ4jAOhPCyT4tlc130_assertion
dcterms:description
"[Some data suggest that the risk for spina bifida associated with C677T homozygosity may depend on nutritional status (e.g., blood folate levels, intake of vitamins) or on the genotype of other folate-related genes (e.g., cystathionine-beta-synthase and methionine synthase reductase).]. 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:10791559
;
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:NP210029.RA80nAJEqYdh0Qw0EuazTWvpi8gX4IQQ4jAOhPCyT4tlc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:55+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" .
}