@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP296345.RAKk6uIDVtBIC_FO76LfH6sB4WCIBUvceErJs_PXghsJw
> .
@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:NP296345.RAKk6uIDVtBIC_FO76LfH6sB4WCIBUvceErJs_PXghsJw130_head
{
this:
np:hasAssertion
dgn-np:NP296345.RAKk6uIDVtBIC_FO76LfH6sB4WCIBUvceErJs_PXghsJw130_assertion
;
np:hasProvenance
dgn-np:NP296345.RAKk6uIDVtBIC_FO76LfH6sB4WCIBUvceErJs_PXghsJw130_provenance
;
np:hasPublicationInfo
dgn-np:NP296345.RAKk6uIDVtBIC_FO76LfH6sB4WCIBUvceErJs_PXghsJw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP296345.RAKk6uIDVtBIC_FO76LfH6sB4WCIBUvceErJs_PXghsJw130_assertion
a
np:Assertion
.
dgn-np:NP296345.RAKk6uIDVtBIC_FO76LfH6sB4WCIBUvceErJs_PXghsJw130_provenance
a
np:Provenance
.
dgn-np:NP296345.RAKk6uIDVtBIC_FO76LfH6sB4WCIBUvceErJs_PXghsJw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP296345.RAKk6uIDVtBIC_FO76LfH6sB4WCIBUvceErJs_PXghsJw130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0040038
a
ncit:C7057
.
dgn-gda:DGNd5773f8cca38993251a286c86ad84be4
sio:SIO_000628
miriam-gene:4524
,
lld:C0040038
;
a
sio:SIO_001122
.
}
dgn-np:NP296345.RAKk6uIDVtBIC_FO76LfH6sB4WCIBUvceErJs_PXghsJw130_provenance
{
dgn-np:NP296345.RAKk6uIDVtBIC_FO76LfH6sB4WCIBUvceErJs_PXghsJw130_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:NP296345.RAKk6uIDVtBIC_FO76LfH6sB4WCIBUvceErJs_PXghsJw130_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" .
}