@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP68204.RAUeuJ-YuARq1yn2wZM0BQdwJq6KKj1KFlVe2Gd1ip6SA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP68204.RAUeuJ-YuARq1yn2wZM0BQdwJq6KKj1KFlVe2Gd1ip6SA130_head
{
this:
np:hasAssertion
dgn-np:NP68204.RAUeuJ-YuARq1yn2wZM0BQdwJq6KKj1KFlVe2Gd1ip6SA130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP68204.RAUeuJ-YuARq1yn2wZM0BQdwJq6KKj1KFlVe2Gd1ip6SA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP68204.RAUeuJ-YuARq1yn2wZM0BQdwJq6KKj1KFlVe2Gd1ip6SA130_assertion
a
np:Assertion
.
dgn-np:NP68204.RAUeuJ-YuARq1yn2wZM0BQdwJq6KKj1KFlVe2Gd1ip6SA130_provenance
a
np:Provenance
.
dgn-np:NP68204.RAUeuJ-YuARq1yn2wZM0BQdwJq6KKj1KFlVe2Gd1ip6SA130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:931
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGNee4be3ee2b16a4b88a015299e627cdc3
sio:SIO_000628
miriam-gene:931
,
lld:C0027051
;
a
sio:SIO_001122
.
}
dgn-np:NP68204.RAUeuJ-YuARq1yn2wZM0BQdwJq6KKj1KFlVe2Gd1ip6SA130_provenance
{
dgn-np:NP68204.RAUeuJ-YuARq1yn2wZM0BQdwJq6KKj1KFlVe2Gd1ip6SA130_assertion
dcterms:description
"[ Gene mutations as CBS 844ins 68, MS A2756G and MTHFR C677T may not be independent risk factors for ischemic cardiovascular and cerebrovascular disease in Southern Chinese Han population. The prevalences of CBS 844ins 68 and MS A2756G may vary with differ]. 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:11758232
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP68204.RAUeuJ-YuARq1yn2wZM0BQdwJq6KKj1KFlVe2Gd1ip6SA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:17+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
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;
pav:authoredBy
<
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> , <
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> , <
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
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pav:version
"v3.0.0" .
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