@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ
> .
@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:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_head
{
this:
np:hasAssertion
dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_assertion
;
np:hasProvenance
dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_assertion
a
np:Assertion
.
dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_provenance
a
np:Provenance
.
dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0034065
a
ncit:C7057
.
dgn-gda:DGN487c90b2853c1f1995f8aedeb55c0c1e
sio:SIO_000628
miriam-gene:4524
,
lld:C0034065
;
a
sio:SIO_001121
.
}
dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_provenance
{
dgn-np:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_assertion
dcterms:description
"[We measured concentrations of homocysteine, methionine, and folate in plasma, total folate and methylfolate in red-blood cells, and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T genotype and other known risk factors for venous thromboembolic disease in 243 patients with deep vein thrombosis or pulmonary embolism and controls matched for sex and age.]. 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:11888585
;
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:NP684036.RAzaZvDpGt52Esuo2S0erS_mufrWipZKZ-M3Uw0FuhoXQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:55+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" .
}