@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP276155.RArPuIB7JFqlZq2KU-aoUEfTasM2hisHWmsyVnjFq0-uc
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
dgn-np:NP276155.RArPuIB7JFqlZq2KU-aoUEfTasM2hisHWmsyVnjFq0-uc130_provenance
;
np:hasPublicationInfo
dgn-np:NP276155.RArPuIB7JFqlZq2KU-aoUEfTasM2hisHWmsyVnjFq0-uc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP276155.RArPuIB7JFqlZq2KU-aoUEfTasM2hisHWmsyVnjFq0-uc130_assertion
a
np:Assertion
.
dgn-np:NP276155.RArPuIB7JFqlZq2KU-aoUEfTasM2hisHWmsyVnjFq0-uc130_provenance
a
np:Provenance
.
dgn-np:NP276155.RArPuIB7JFqlZq2KU-aoUEfTasM2hisHWmsyVnjFq0-uc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP276155.RArPuIB7JFqlZq2KU-aoUEfTasM2hisHWmsyVnjFq0-uc130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN8ae7ef281bd8753e063e1c8288b653bc
sio:SIO_000628
miriam-gene:4524
,
lld:C0027051
;
a
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.
}
dgn-np:NP276155.RArPuIB7JFqlZq2KU-aoUEfTasM2hisHWmsyVnjFq0-uc130_provenance
{
dgn-np:NP276155.RArPuIB7JFqlZq2KU-aoUEfTasM2hisHWmsyVnjFq0-uc130_assertion
dcterms:description
"[In the present study, we have investigated the frequency of the MTHFR C677T, CBS 844ins68, and MS A2756G mutations in 102 patients with ischemic stroke (IS), 73 patients with myocardial infarction (MI) and 100 healthy controls.]. 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:11672761
;
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 .
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dgn-np:NP276155.RArPuIB7JFqlZq2KU-aoUEfTasM2hisHWmsyVnjFq0-uc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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