@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP778462.RAte6VZWw3iSirhB-9sz31HvNjGHq7yoRZPqPaZpeWFdQ
> .
@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:NP778462.RAte6VZWw3iSirhB-9sz31HvNjGHq7yoRZPqPaZpeWFdQ130_head
{
this:
np:hasAssertion
dgn-np:NP778462.RAte6VZWw3iSirhB-9sz31HvNjGHq7yoRZPqPaZpeWFdQ130_assertion
;
np:hasProvenance
dgn-np:NP778462.RAte6VZWw3iSirhB-9sz31HvNjGHq7yoRZPqPaZpeWFdQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP778462.RAte6VZWw3iSirhB-9sz31HvNjGHq7yoRZPqPaZpeWFdQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP778462.RAte6VZWw3iSirhB-9sz31HvNjGHq7yoRZPqPaZpeWFdQ130_assertion
a
np:Assertion
.
dgn-np:NP778462.RAte6VZWw3iSirhB-9sz31HvNjGHq7yoRZPqPaZpeWFdQ130_provenance
a
np:Provenance
.
dgn-np:NP778462.RAte6VZWw3iSirhB-9sz31HvNjGHq7yoRZPqPaZpeWFdQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP778462.RAte6VZWw3iSirhB-9sz31HvNjGHq7yoRZPqPaZpeWFdQ130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0025312
a
ncit:C7057
.
dgn-gda:DGNdcb4f0a15fe2cd6e42fe8dd87c705478
sio:SIO_000628
miriam-gene:4524
,
lld:C0025312
;
a
sio:SIO_001121
.
}
dgn-np:NP778462.RAte6VZWw3iSirhB-9sz31HvNjGHq7yoRZPqPaZpeWFdQ130_provenance
{
dgn-np:NP778462.RAte6VZWw3iSirhB-9sz31HvNjGHq7yoRZPqPaZpeWFdQ130_assertion
dcterms:description
"[To evaluate the relationship between genotypes of methylene tetrahydrofolate reductase (MTHFR), and plasma folate and homocysteine (Hcy) levels in meningomyelocele, 21 Korean patients, 47 of their family members, and 43 healthy controls were recruited.]. 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:11048629
;
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:NP778462.RAte6VZWw3iSirhB-9sz31HvNjGHq7yoRZPqPaZpeWFdQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}