@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP286776.RA3r118_Gg_xsh0rC6Czz1qp9uZgOnMvin7Yn6e7c1sQk
> .
@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/v3.0.0/void/
> .
dgn-np:NP286776.RA3r118_Gg_xsh0rC6Czz1qp9uZgOnMvin7Yn6e7c1sQk130_head
{
this:
np:hasAssertion
dgn-np:NP286776.RA3r118_Gg_xsh0rC6Czz1qp9uZgOnMvin7Yn6e7c1sQk130_assertion
;
np:hasProvenance
dgn-np:NP286776.RA3r118_Gg_xsh0rC6Czz1qp9uZgOnMvin7Yn6e7c1sQk130_provenance
;
np:hasPublicationInfo
dgn-np:NP286776.RA3r118_Gg_xsh0rC6Czz1qp9uZgOnMvin7Yn6e7c1sQk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP286776.RA3r118_Gg_xsh0rC6Czz1qp9uZgOnMvin7Yn6e7c1sQk130_assertion
a
np:Assertion
.
dgn-np:NP286776.RA3r118_Gg_xsh0rC6Czz1qp9uZgOnMvin7Yn6e7c1sQk130_provenance
a
np:Provenance
.
dgn-np:NP286776.RA3r118_Gg_xsh0rC6Czz1qp9uZgOnMvin7Yn6e7c1sQk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP286776.RA3r118_Gg_xsh0rC6Czz1qp9uZgOnMvin7Yn6e7c1sQk130_assertion
{
miriam-gene:875
a
ncit:C16612
.
lld:C0040038
a
ncit:C7057
.
dgn-gda:DGN684762aa39680bcd0cc30c86e2fa270f
sio:SIO_000628
miriam-gene:875
,
lld:C0040038
;
a
sio:SIO_001122
.
}
dgn-np:NP286776.RA3r118_Gg_xsh0rC6Czz1qp9uZgOnMvin7Yn6e7c1sQk130_provenance
{
dgn-np:NP286776.RA3r118_Gg_xsh0rC6Czz1qp9uZgOnMvin7Yn6e7c1sQk130_assertion
dcterms:description
"[The frequency of the heterozygous 844ins68 mutation of the cystathionine beta-synthase (CBS) gene and of its association with the homozygous C677T transition of the methylenetetrahydrofolate reductase (MTHFR) gene, plasma fasting tHcy, folate and vitamin B12 levels were evaluated in 309 consecutive patients with objectively diagnosed early-onset venous (n = 200) or arterial thromboembolic disease (n = 109) recruited over 25 months in Milan (North Italy) and Naples (South Italy).]. 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:11057853
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP286776.RA3r118_Gg_xsh0rC6Czz1qp9uZgOnMvin7Yn6e7c1sQk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:23+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}