@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP159701.RAjNGc7XriB9mGItBCi27MObPzcKRBlmdt4lhzWb9uAQ4
> .
@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:NP159701.RAjNGc7XriB9mGItBCi27MObPzcKRBlmdt4lhzWb9uAQ4130_head
{
this:
np:hasAssertion
dgn-np:NP159701.RAjNGc7XriB9mGItBCi27MObPzcKRBlmdt4lhzWb9uAQ4130_assertion
;
np:hasProvenance
dgn-np:NP159701.RAjNGc7XriB9mGItBCi27MObPzcKRBlmdt4lhzWb9uAQ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP159701.RAjNGc7XriB9mGItBCi27MObPzcKRBlmdt4lhzWb9uAQ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP159701.RAjNGc7XriB9mGItBCi27MObPzcKRBlmdt4lhzWb9uAQ4130_assertion
a
np:Assertion
.
dgn-np:NP159701.RAjNGc7XriB9mGItBCi27MObPzcKRBlmdt4lhzWb9uAQ4130_provenance
a
np:Provenance
.
dgn-np:NP159701.RAjNGc7XriB9mGItBCi27MObPzcKRBlmdt4lhzWb9uAQ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP159701.RAjNGc7XriB9mGItBCi27MObPzcKRBlmdt4lhzWb9uAQ4130_assertion
{
miriam-gene:353
a
ncit:C16612
.
lld:C0018801
a
ncit:C7057
.
dgn-gda:DGN5e09ec6c57693577ea4dcead06f853a3
sio:SIO_000628
miriam-gene:353
,
lld:C0018801
;
a
sio:SIO_001121
.
}
dgn-np:NP159701.RAjNGc7XriB9mGItBCi27MObPzcKRBlmdt4lhzWb9uAQ4130_provenance
{
dgn-np:NP159701.RAjNGc7XriB9mGItBCi27MObPzcKRBlmdt4lhzWb9uAQ4130_assertion
dcterms:description
"[Possession of the C34T mutation in AMP deaminase (AMPD1) gene has been shown to be associated with attenuation of the progression of heart failure and improved survival in ischemic heart 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:16021915
;
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:NP159701.RAjNGc7XriB9mGItBCi27MObPzcKRBlmdt4lhzWb9uAQ4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+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" .
}