@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP738859.RA4fOfMba2drcOAvclXIxuY1_CCJPjLvh8WNNsKlYsTDA
> .
@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:NP738859.RA4fOfMba2drcOAvclXIxuY1_CCJPjLvh8WNNsKlYsTDA130_head
{
this:
np:hasAssertion
dgn-np:NP738859.RA4fOfMba2drcOAvclXIxuY1_CCJPjLvh8WNNsKlYsTDA130_assertion
;
np:hasProvenance
dgn-np:NP738859.RA4fOfMba2drcOAvclXIxuY1_CCJPjLvh8WNNsKlYsTDA130_provenance
;
np:hasPublicationInfo
dgn-np:NP738859.RA4fOfMba2drcOAvclXIxuY1_CCJPjLvh8WNNsKlYsTDA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP738859.RA4fOfMba2drcOAvclXIxuY1_CCJPjLvh8WNNsKlYsTDA130_assertion
a
np:Assertion
.
dgn-np:NP738859.RA4fOfMba2drcOAvclXIxuY1_CCJPjLvh8WNNsKlYsTDA130_provenance
a
np:Provenance
.
dgn-np:NP738859.RA4fOfMba2drcOAvclXIxuY1_CCJPjLvh8WNNsKlYsTDA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP738859.RA4fOfMba2drcOAvclXIxuY1_CCJPjLvh8WNNsKlYsTDA130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0005586
a
ncit:C7057
.
dgn-gda:DGNd4682611af4dbb5b721b05bc9a0cbfb7
sio:SIO_000628
miriam-gene:4524
,
lld:C0005586
;
a
sio:SIO_001121
.
}
dgn-np:NP738859.RA4fOfMba2drcOAvclXIxuY1_CCJPjLvh8WNNsKlYsTDA130_provenance
{
dgn-np:NP738859.RA4fOfMba2drcOAvclXIxuY1_CCJPjLvh8WNNsKlYsTDA130_assertion
dcterms:description
"[Since a common variant of the MTHFR gene, T677(Ala), responsible for the thermolabile MTHFR with less than 50% specific MTHFR activity, has been reported, we examined whether the T677 allele is associated with psychiatric disorders in an unrelated Japanese population consisting of 297 schizophrenics, 32 patients with major depression, 40 patients with bipolar disorder, and 419 controls.]. 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:9342205
;
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:NP738859.RA4fOfMba2drcOAvclXIxuY1_CCJPjLvh8WNNsKlYsTDA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:28+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" .
}