@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP477044.RAEuhhkKSn0NBuHwePcQ8H8SrFWvH-HduK3rhP2GnnRaQ
> .
@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:NP477044.RAEuhhkKSn0NBuHwePcQ8H8SrFWvH-HduK3rhP2GnnRaQ130_head
{
this:
np:hasAssertion
dgn-np:NP477044.RAEuhhkKSn0NBuHwePcQ8H8SrFWvH-HduK3rhP2GnnRaQ130_assertion
;
np:hasProvenance
dgn-np:NP477044.RAEuhhkKSn0NBuHwePcQ8H8SrFWvH-HduK3rhP2GnnRaQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP477044.RAEuhhkKSn0NBuHwePcQ8H8SrFWvH-HduK3rhP2GnnRaQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP477044.RAEuhhkKSn0NBuHwePcQ8H8SrFWvH-HduK3rhP2GnnRaQ130_assertion
a
np:Assertion
.
dgn-np:NP477044.RAEuhhkKSn0NBuHwePcQ8H8SrFWvH-HduK3rhP2GnnRaQ130_provenance
a
np:Provenance
.
dgn-np:NP477044.RAEuhhkKSn0NBuHwePcQ8H8SrFWvH-HduK3rhP2GnnRaQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP477044.RAEuhhkKSn0NBuHwePcQ8H8SrFWvH-HduK3rhP2GnnRaQ130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0011570
a
ncit:C7057
.
dgn-gda:DGNbd3d755b0fb5f45460ba35e56216d5fa
sio:SIO_000628
miriam-gene:4524
,
lld:C0011570
;
a
sio:SIO_001121
.
}
dgn-np:NP477044.RAEuhhkKSn0NBuHwePcQ8H8SrFWvH-HduK3rhP2GnnRaQ130_provenance
{
dgn-np:NP477044.RAEuhhkKSn0NBuHwePcQ8H8SrFWvH-HduK3rhP2GnnRaQ130_assertion
dcterms:description
"[We used a series of neuro-psychological tests to examine the association of the MTHFR C677T polymorphism with cognition and depression and also to assess whether genotype modifies the association of folate and homocysteine with these outcomes.]. 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:22739363
;
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:NP477044.RAEuhhkKSn0NBuHwePcQ8H8SrFWvH-HduK3rhP2GnnRaQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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" .
}