@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP913771.RAenPso2_pw2HYUpEUdUvvIIx8FZCCBdZ5wum5ab75zdw
> .
@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:NP913771.RAenPso2_pw2HYUpEUdUvvIIx8FZCCBdZ5wum5ab75zdw130_head
{
this:
np:hasAssertion
dgn-np:NP913771.RAenPso2_pw2HYUpEUdUvvIIx8FZCCBdZ5wum5ab75zdw130_assertion
;
np:hasProvenance
dgn-np:NP913771.RAenPso2_pw2HYUpEUdUvvIIx8FZCCBdZ5wum5ab75zdw130_provenance
;
np:hasPublicationInfo
dgn-np:NP913771.RAenPso2_pw2HYUpEUdUvvIIx8FZCCBdZ5wum5ab75zdw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP913771.RAenPso2_pw2HYUpEUdUvvIIx8FZCCBdZ5wum5ab75zdw130_assertion
a
np:Assertion
.
dgn-np:NP913771.RAenPso2_pw2HYUpEUdUvvIIx8FZCCBdZ5wum5ab75zdw130_provenance
a
np:Provenance
.
dgn-np:NP913771.RAenPso2_pw2HYUpEUdUvvIIx8FZCCBdZ5wum5ab75zdw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP913771.RAenPso2_pw2HYUpEUdUvvIIx8FZCCBdZ5wum5ab75zdw130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0085096
a
ncit:C7057
.
dgn-gda:DGN2da78d92311e7a1b2c6efa6970c29077
sio:SIO_000628
miriam-gene:4524
,
lld:C0085096
;
a
sio:SIO_001121
.
}
dgn-np:NP913771.RAenPso2_pw2HYUpEUdUvvIIx8FZCCBdZ5wum5ab75zdw130_provenance
{
dgn-np:NP913771.RAenPso2_pw2HYUpEUdUvvIIx8FZCCBdZ5wum5ab75zdw130_assertion
dcterms:description
"[The prevalence of peripheral vascular disease increased with the incidence of MTHFR C677T mutations for all patients, and the incidence of cerebrovascular accidents also increased with the presence of mutations for young patients (≤ 60 yr) (P < 0.05).]. 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:21394321
;
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:NP913771.RAenPso2_pw2HYUpEUdUvvIIx8FZCCBdZ5wum5ab75zdw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:20+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" .
}