@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP506078.RAmhEQ0pCPe3lQxRpEgE03EFfHX5_549q3IxextsXG3rY
> .
@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:NP506078.RAmhEQ0pCPe3lQxRpEgE03EFfHX5_549q3IxextsXG3rY130_head
{
this:
np:hasAssertion
dgn-np:NP506078.RAmhEQ0pCPe3lQxRpEgE03EFfHX5_549q3IxextsXG3rY130_assertion
;
np:hasProvenance
dgn-np:NP506078.RAmhEQ0pCPe3lQxRpEgE03EFfHX5_549q3IxextsXG3rY130_provenance
;
np:hasPublicationInfo
dgn-np:NP506078.RAmhEQ0pCPe3lQxRpEgE03EFfHX5_549q3IxextsXG3rY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP506078.RAmhEQ0pCPe3lQxRpEgE03EFfHX5_549q3IxextsXG3rY130_assertion
a
np:Assertion
.
dgn-np:NP506078.RAmhEQ0pCPe3lQxRpEgE03EFfHX5_549q3IxextsXG3rY130_provenance
a
np:Provenance
.
dgn-np:NP506078.RAmhEQ0pCPe3lQxRpEgE03EFfHX5_549q3IxextsXG3rY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP506078.RAmhEQ0pCPe3lQxRpEgE03EFfHX5_549q3IxextsXG3rY130_assertion
{
miriam-gene:4282
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN86912a3120438b2abc5c152233057f4d
sio:SIO_000628
miriam-gene:4282
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP506078.RAmhEQ0pCPe3lQxRpEgE03EFfHX5_549q3IxextsXG3rY130_provenance
{
dgn-np:NP506078.RAmhEQ0pCPe3lQxRpEgE03EFfHX5_549q3IxextsXG3rY130_assertion
dcterms:description
"[We anticipate that genetic variation in MIF expression may impact on the response of the human heart to ischaemia by the AMPK pathway, and that diagnostic MIF genotyping might predict risk in patients with coronary artery 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:18235500
;
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:NP506078.RAmhEQ0pCPe3lQxRpEgE03EFfHX5_549q3IxextsXG3rY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:02+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" .
}