@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP726179.RArWq1LzDKngXNx8UFkXpVrB4UI1CwLSiyK0LKz_Wp6mU
> .
@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:NP726179.RArWq1LzDKngXNx8UFkXpVrB4UI1CwLSiyK0LKz_Wp6mU130_head
{
this:
np:hasAssertion
dgn-np:NP726179.RArWq1LzDKngXNx8UFkXpVrB4UI1CwLSiyK0LKz_Wp6mU130_assertion
;
np:hasProvenance
dgn-np:NP726179.RArWq1LzDKngXNx8UFkXpVrB4UI1CwLSiyK0LKz_Wp6mU130_provenance
;
np:hasPublicationInfo
dgn-np:NP726179.RArWq1LzDKngXNx8UFkXpVrB4UI1CwLSiyK0LKz_Wp6mU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP726179.RArWq1LzDKngXNx8UFkXpVrB4UI1CwLSiyK0LKz_Wp6mU130_assertion
a
np:Assertion
.
dgn-np:NP726179.RArWq1LzDKngXNx8UFkXpVrB4UI1CwLSiyK0LKz_Wp6mU130_provenance
a
np:Provenance
.
dgn-np:NP726179.RArWq1LzDKngXNx8UFkXpVrB4UI1CwLSiyK0LKz_Wp6mU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP726179.RArWq1LzDKngXNx8UFkXpVrB4UI1CwLSiyK0LKz_Wp6mU130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0577631
a
ncit:C7057
.
dgn-gda:DGN6d342893a71a1df194c8e8b1564d1246
sio:SIO_000628
miriam-gene:4524
,
lld:C0577631
;
a
sio:SIO_001121
.
}
dgn-np:NP726179.RArWq1LzDKngXNx8UFkXpVrB4UI1CwLSiyK0LKz_Wp6mU130_provenance
{
dgn-np:NP726179.RArWq1LzDKngXNx8UFkXpVrB4UI1CwLSiyK0LKz_Wp6mU130_assertion
dcterms:description
"[CONCLUISONS: Thus, plasma H(e), but not MTHFR genotype, is significantly associated with carotid atherosclerosis, suggesting that the biochemical test may be sufficient to identify patients who may be at increased risk of atherosclerosis through this mechanism.]. 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:10229729
;
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:NP726179.RArWq1LzDKngXNx8UFkXpVrB4UI1CwLSiyK0LKz_Wp6mU130_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" .
}