@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP314854.RAK8H6L2UlRxUTqKjtvBku3fEoMd3I1hhRdu1EDAwFLnA
> .
@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:NP314854.RAK8H6L2UlRxUTqKjtvBku3fEoMd3I1hhRdu1EDAwFLnA130_head
{
this:
np:hasAssertion
dgn-np:NP314854.RAK8H6L2UlRxUTqKjtvBku3fEoMd3I1hhRdu1EDAwFLnA130_assertion
;
np:hasProvenance
dgn-np:NP314854.RAK8H6L2UlRxUTqKjtvBku3fEoMd3I1hhRdu1EDAwFLnA130_provenance
;
np:hasPublicationInfo
dgn-np:NP314854.RAK8H6L2UlRxUTqKjtvBku3fEoMd3I1hhRdu1EDAwFLnA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP314854.RAK8H6L2UlRxUTqKjtvBku3fEoMd3I1hhRdu1EDAwFLnA130_assertion
a
np:Assertion
.
dgn-np:NP314854.RAK8H6L2UlRxUTqKjtvBku3fEoMd3I1hhRdu1EDAwFLnA130_provenance
a
np:Provenance
.
dgn-np:NP314854.RAK8H6L2UlRxUTqKjtvBku3fEoMd3I1hhRdu1EDAwFLnA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP314854.RAK8H6L2UlRxUTqKjtvBku3fEoMd3I1hhRdu1EDAwFLnA130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN852b1cb2fb4c260ff2fb4ef93ff7c251
sio:SIO_000628
miriam-gene:2147
,
lld:C0027051
;
a
sio:SIO_001121
.
}
dgn-np:NP314854.RAK8H6L2UlRxUTqKjtvBku3fEoMd3I1hhRdu1EDAwFLnA130_provenance
{
dgn-np:NP314854.RAK8H6L2UlRxUTqKjtvBku3fEoMd3I1hhRdu1EDAwFLnA130_assertion
dcterms:description
"[FV Leiden, prothrombin 20210 variant, and MTHFR mutation are no risk factors for left ventricular thrombus in patients with myocardial infarction.The presence of multiple mutations did not influence the development and outcome of LV thrombus in patients with myocardial infarction]. 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:15030132
;
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:NP314854.RAK8H6L2UlRxUTqKjtvBku3fEoMd3I1hhRdu1EDAwFLnA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:00+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: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" .
}