@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP198641.RAsqgr7ukx7ZSrnUO5YhQQ566lHzsVFy4A3MU6aiV_fWg
> .
@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:NP198641.RAsqgr7ukx7ZSrnUO5YhQQ566lHzsVFy4A3MU6aiV_fWg130_head
{
this:
np:hasAssertion
dgn-np:NP198641.RAsqgr7ukx7ZSrnUO5YhQQ566lHzsVFy4A3MU6aiV_fWg130_assertion
;
np:hasProvenance
dgn-np:NP198641.RAsqgr7ukx7ZSrnUO5YhQQ566lHzsVFy4A3MU6aiV_fWg130_provenance
;
np:hasPublicationInfo
dgn-np:NP198641.RAsqgr7ukx7ZSrnUO5YhQQ566lHzsVFy4A3MU6aiV_fWg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP198641.RAsqgr7ukx7ZSrnUO5YhQQ566lHzsVFy4A3MU6aiV_fWg130_assertion
a
np:Assertion
.
dgn-np:NP198641.RAsqgr7ukx7ZSrnUO5YhQQ566lHzsVFy4A3MU6aiV_fWg130_provenance
a
np:Provenance
.
dgn-np:NP198641.RAsqgr7ukx7ZSrnUO5YhQQ566lHzsVFy4A3MU6aiV_fWg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP198641.RAsqgr7ukx7ZSrnUO5YhQQ566lHzsVFy4A3MU6aiV_fWg130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGNf1cb336c7a6db908b140591957396d17
sio:SIO_000628
miriam-gene:4524
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP198641.RAsqgr7ukx7ZSrnUO5YhQQ566lHzsVFy4A3MU6aiV_fWg130_provenance
{
dgn-np:NP198641.RAsqgr7ukx7ZSrnUO5YhQQ566lHzsVFy4A3MU6aiV_fWg130_assertion
dcterms:description
"[These data indicate that the MN index is associated with the severity of CAD and is related to the MTHFR polymorphism, suggesting an interesting link between coronary atherosclerosis and genetic instability in humans.]. 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:12522558
;
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:NP198641.RAsqgr7ukx7ZSrnUO5YhQQ566lHzsVFy4A3MU6aiV_fWg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:49+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" .
}