@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP855176.RACj_MsK0NhllBsbAhdxX3JmkKNLpS2eMoCDEgN_C6-dU
> .
@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:NP855176.RACj_MsK0NhllBsbAhdxX3JmkKNLpS2eMoCDEgN_C6-dU130_head
{
this:
np:hasAssertion
dgn-np:NP855176.RACj_MsK0NhllBsbAhdxX3JmkKNLpS2eMoCDEgN_C6-dU130_assertion
;
np:hasProvenance
dgn-np:NP855176.RACj_MsK0NhllBsbAhdxX3JmkKNLpS2eMoCDEgN_C6-dU130_provenance
;
np:hasPublicationInfo
dgn-np:NP855176.RACj_MsK0NhllBsbAhdxX3JmkKNLpS2eMoCDEgN_C6-dU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP855176.RACj_MsK0NhllBsbAhdxX3JmkKNLpS2eMoCDEgN_C6-dU130_assertion
a
np:Assertion
.
dgn-np:NP855176.RACj_MsK0NhllBsbAhdxX3JmkKNLpS2eMoCDEgN_C6-dU130_provenance
a
np:Provenance
.
dgn-np:NP855176.RACj_MsK0NhllBsbAhdxX3JmkKNLpS2eMoCDEgN_C6-dU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP855176.RACj_MsK0NhllBsbAhdxX3JmkKNLpS2eMoCDEgN_C6-dU130_assertion
{
miriam-gene:4709
a
ncit:C16612
.
lld:C0042373
a
ncit:C7057
.
dgn-gda:DGN912f538f2a70254908bf4fb5098f7853
sio:SIO_000628
miriam-gene:4709
,
lld:C0042373
;
a
sio:SIO_001121
.
}
dgn-np:NP855176.RACj_MsK0NhllBsbAhdxX3JmkKNLpS2eMoCDEgN_C6-dU130_provenance
{
dgn-np:NP855176.RACj_MsK0NhllBsbAhdxX3JmkKNLpS2eMoCDEgN_C6-dU130_assertion
dcterms:description
"[Hyperhomocysteinemia, a risk factor for vascular disease, is related to vitamin B12, vitamin B6, and especially folate deficiency, or to genetic factors such as mutations in methylenetetrahydrofolate reductase (MTHFR), an enzyme involved in the remethylation pathway of homocysteine to methionine.]. 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:9826223
;
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:NP855176.RACj_MsK0NhllBsbAhdxX3JmkKNLpS2eMoCDEgN_C6-dU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:43+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" .
}