@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4
> .
@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:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_head
{
this:
np:hasAssertion
dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_assertion
;
np:hasProvenance
dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_provenance
;
np:hasPublicationInfo
dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_assertion
a
np:Assertion
.
dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_provenance
a
np:Provenance
.
dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0042373
a
ncit:C7057
.
dgn-gda:DGN37e8a43aa026f3843bc587ed28518e78
sio:SIO_000628
miriam-gene:4524
,
lld:C0042373
;
a
sio:SIO_001121
.
}
dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_provenance
{
dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_assertion
dcterms:description
"[These data suggest that in selected patients homozygosity for the MTHFR mutation increases the risk of both arterial and venous thromboses and that differences in selection criteria for the patient group may be responsible in part for the controversial association of the MTHFR mutation and vascular disease.]. 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:10477457
;
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:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:45+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" .
}