@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP725903.RAhfSGfOow0qHzc_YYBjlygwyC07hq_na8AhxhI0t9TzQ
> .
@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:NP725903.RAhfSGfOow0qHzc_YYBjlygwyC07hq_na8AhxhI0t9TzQ130_head
{
this:
np:hasAssertion
dgn-np:NP725903.RAhfSGfOow0qHzc_YYBjlygwyC07hq_na8AhxhI0t9TzQ130_assertion
;
np:hasProvenance
dgn-np:NP725903.RAhfSGfOow0qHzc_YYBjlygwyC07hq_na8AhxhI0t9TzQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP725903.RAhfSGfOow0qHzc_YYBjlygwyC07hq_na8AhxhI0t9TzQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP725903.RAhfSGfOow0qHzc_YYBjlygwyC07hq_na8AhxhI0t9TzQ130_assertion
a
np:Assertion
.
dgn-np:NP725903.RAhfSGfOow0qHzc_YYBjlygwyC07hq_na8AhxhI0t9TzQ130_provenance
a
np:Provenance
.
dgn-np:NP725903.RAhfSGfOow0qHzc_YYBjlygwyC07hq_na8AhxhI0t9TzQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP725903.RAhfSGfOow0qHzc_YYBjlygwyC07hq_na8AhxhI0t9TzQ130_assertion
{
miriam-gene:2762
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGN037a4fdbdc91513adc8bd1445903c5ed
sio:SIO_000628
miriam-gene:2762
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP725903.RAhfSGfOow0qHzc_YYBjlygwyC07hq_na8AhxhI0t9TzQ130_provenance
{
dgn-np:NP725903.RAhfSGfOow0qHzc_YYBjlygwyC07hq_na8AhxhI0t9TzQ130_assertion
dcterms:description
"[Further analysis on gray matter density (GMD) revealed significant diagnostic effects in bilateral frontal cortices, bilateral insula, left medial temporal cortex and bilateral occipital cortices, effects of MTHFR genotype in the right insula, right inferior frontal gyrus, right rolandic opercula, right parahippocampal gyrus and right medial temporal pole, and effects of genotype-diagnosis interaction in the right temporal gyrus.]. 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:23318463
;
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:NP725903.RAhfSGfOow0qHzc_YYBjlygwyC07hq_na8AhxhI0t9TzQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}