@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP261512.RAtnr_u-JvBkPTJLHzuqDm8aCHdWO75JmVIL-zCQHj5wk
> .
@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:NP261512.RAtnr_u-JvBkPTJLHzuqDm8aCHdWO75JmVIL-zCQHj5wk130_head
{
this:
np:hasAssertion
dgn-np:NP261512.RAtnr_u-JvBkPTJLHzuqDm8aCHdWO75JmVIL-zCQHj5wk130_assertion
;
np:hasProvenance
dgn-np:NP261512.RAtnr_u-JvBkPTJLHzuqDm8aCHdWO75JmVIL-zCQHj5wk130_provenance
;
np:hasPublicationInfo
dgn-np:NP261512.RAtnr_u-JvBkPTJLHzuqDm8aCHdWO75JmVIL-zCQHj5wk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP261512.RAtnr_u-JvBkPTJLHzuqDm8aCHdWO75JmVIL-zCQHj5wk130_assertion
a
np:Assertion
.
dgn-np:NP261512.RAtnr_u-JvBkPTJLHzuqDm8aCHdWO75JmVIL-zCQHj5wk130_provenance
a
np:Provenance
.
dgn-np:NP261512.RAtnr_u-JvBkPTJLHzuqDm8aCHdWO75JmVIL-zCQHj5wk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP261512.RAtnr_u-JvBkPTJLHzuqDm8aCHdWO75JmVIL-zCQHj5wk130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0598608
a
ncit:C7057
.
dgn-gda:DGN2eb3560464ddeb2e36ce70219abfded4
sio:SIO_000628
miriam-gene:4846
,
lld:C0598608
;
a
sio:SIO_001121
.
}
dgn-np:NP261512.RAtnr_u-JvBkPTJLHzuqDm8aCHdWO75JmVIL-zCQHj5wk130_provenance
{
dgn-np:NP261512.RAtnr_u-JvBkPTJLHzuqDm8aCHdWO75JmVIL-zCQHj5wk130_assertion
dcterms:description
"[In this study, we evaluated the relationships between plasma homocysteine levels and genetic risk factors for hyperhomocysteinemia, i.e., the presence of gene variants for methylenetetrahydrofolate reductase (MTHFR) and endothelial nitric oxide synthase (eNOS) in patients with cognitive impairment.]. 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:21607713
;
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:NP261512.RAtnr_u-JvBkPTJLHzuqDm8aCHdWO75JmVIL-zCQHj5wk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:26+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" .
}