@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP374002.RAATjm1Xo8SuXfbRhAwWOLhWDPUBIfBY4BTTDxmn-I7mE
> .
@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 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:NP374002.RAATjm1Xo8SuXfbRhAwWOLhWDPUBIfBY4BTTDxmn-I7mE130_head
{
this:
np:hasAssertion
dgn-np:NP374002.RAATjm1Xo8SuXfbRhAwWOLhWDPUBIfBY4BTTDxmn-I7mE130_assertion
;
np:hasProvenance
dgn-np:NP374002.RAATjm1Xo8SuXfbRhAwWOLhWDPUBIfBY4BTTDxmn-I7mE130_provenance
;
np:hasPublicationInfo
dgn-np:NP374002.RAATjm1Xo8SuXfbRhAwWOLhWDPUBIfBY4BTTDxmn-I7mE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP374002.RAATjm1Xo8SuXfbRhAwWOLhWDPUBIfBY4BTTDxmn-I7mE130_assertion
a
np:Assertion
.
dgn-np:NP374002.RAATjm1Xo8SuXfbRhAwWOLhWDPUBIfBY4BTTDxmn-I7mE130_provenance
a
np:Provenance
.
dgn-np:NP374002.RAATjm1Xo8SuXfbRhAwWOLhWDPUBIfBY4BTTDxmn-I7mE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP374002.RAATjm1Xo8SuXfbRhAwWOLhWDPUBIfBY4BTTDxmn-I7mE130_assertion
{
miriam-gene:4709
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNdf23c8f52a9b6dfb195d9b073636b8e1
sio:SIO_000628
miriam-gene:4709
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP374002.RAATjm1Xo8SuXfbRhAwWOLhWDPUBIfBY4BTTDxmn-I7mE130_provenance
{
dgn-np:NP374002.RAATjm1Xo8SuXfbRhAwWOLhWDPUBIfBY4BTTDxmn-I7mE130_assertion
dc:description
"[In this study, we measured serum folate, serum vitamin B12, and plasma homocysteine and determined the MTHFR C677T genotype of 78 patients with essential hypertension, 100 patients with coronary artery disease, and 100 healthy subjects.]. 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:18068006
;
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:NP374002.RAATjm1Xo8SuXfbRhAwWOLhWDPUBIfBY4BTTDxmn-I7mE130_publicationInfo
{
this:
dc:created
"2014-10-02T12:35:39+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}