@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP296349.RABzDhoE7RqjDj9fukFbmhHvteEnSBgAKAjpoj9pmK_ZQ
> .
@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/v4.0.0/void/
> .
dgn-np:NP296349.RABzDhoE7RqjDj9fukFbmhHvteEnSBgAKAjpoj9pmK_ZQ130_head
{
this:
np:hasAssertion
dgn-np:NP296349.RABzDhoE7RqjDj9fukFbmhHvteEnSBgAKAjpoj9pmK_ZQ130_assertion
;
np:hasProvenance
dgn-np:NP296349.RABzDhoE7RqjDj9fukFbmhHvteEnSBgAKAjpoj9pmK_ZQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP296349.RABzDhoE7RqjDj9fukFbmhHvteEnSBgAKAjpoj9pmK_ZQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP296349.RABzDhoE7RqjDj9fukFbmhHvteEnSBgAKAjpoj9pmK_ZQ130_assertion
a
np:Assertion
.
dgn-np:NP296349.RABzDhoE7RqjDj9fukFbmhHvteEnSBgAKAjpoj9pmK_ZQ130_provenance
a
np:Provenance
.
dgn-np:NP296349.RABzDhoE7RqjDj9fukFbmhHvteEnSBgAKAjpoj9pmK_ZQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP296349.RABzDhoE7RqjDj9fukFbmhHvteEnSBgAKAjpoj9pmK_ZQ130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0598608
a
ncit:C7057
.
dgn-gda:DGNfd554e175d6742a13813f29d669625c1
sio:SIO_000628
miriam-gene:4524
,
lld:C0598608
;
a
sio:SIO_001122
.
}
dgn-np:NP296349.RABzDhoE7RqjDj9fukFbmhHvteEnSBgAKAjpoj9pmK_ZQ130_provenance
{
dgn-np:NP296349.RABzDhoE7RqjDj9fukFbmhHvteEnSBgAKAjpoj9pmK_ZQ130_assertion
dcterms:description
"[Genotyping for mutations that are possible causes of moderate hyperhomocysteinemia, such as the thermolabile variant (C677T) of methylenetetrahydrofolate reductase (MTHFR), does not seem useful to identify individuals at higher risk for venous thromboembolism.]. 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:11011848
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP296349.RABzDhoE7RqjDj9fukFbmhHvteEnSBgAKAjpoj9pmK_ZQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:00+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}