@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP161846.RA1RcBnKXugXH0rThH_Czs6tc08iGO2Nz0wTXmN8wlrRo
> .
@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:NP161846.RA1RcBnKXugXH0rThH_Czs6tc08iGO2Nz0wTXmN8wlrRo130_head
{
this:
np:hasAssertion
dgn-np:NP161846.RA1RcBnKXugXH0rThH_Czs6tc08iGO2Nz0wTXmN8wlrRo130_assertion
;
np:hasProvenance
dgn-np:NP161846.RA1RcBnKXugXH0rThH_Czs6tc08iGO2Nz0wTXmN8wlrRo130_provenance
;
np:hasPublicationInfo
dgn-np:NP161846.RA1RcBnKXugXH0rThH_Czs6tc08iGO2Nz0wTXmN8wlrRo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP161846.RA1RcBnKXugXH0rThH_Czs6tc08iGO2Nz0wTXmN8wlrRo130_assertion
a
np:Assertion
.
dgn-np:NP161846.RA1RcBnKXugXH0rThH_Czs6tc08iGO2Nz0wTXmN8wlrRo130_provenance
a
np:Provenance
.
dgn-np:NP161846.RA1RcBnKXugXH0rThH_Czs6tc08iGO2Nz0wTXmN8wlrRo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP161846.RA1RcBnKXugXH0rThH_Czs6tc08iGO2Nz0wTXmN8wlrRo130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C2733225
a
ncit:C7057
.
dgn-gda:DGN6fed4a4342d8a73787c69689c0a4f69a
sio:SIO_000628
miriam-gene:4524
,
lld:C2733225
;
a
sio:SIO_001121
.
}
dgn-np:NP161846.RA1RcBnKXugXH0rThH_Czs6tc08iGO2Nz0wTXmN8wlrRo130_provenance
{
dgn-np:NP161846.RA1RcBnKXugXH0rThH_Czs6tc08iGO2Nz0wTXmN8wlrRo130_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:NP161846.RA1RcBnKXugXH0rThH_Czs6tc08iGO2Nz0wTXmN8wlrRo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}