@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP854817.RAMkpO-Ov4CpyUSBIwxz1LhnNqgn3cwn9dS62t9KTVXSc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP854817.RAMkpO-Ov4CpyUSBIwxz1LhnNqgn3cwn9dS62t9KTVXSc130_head
{
this:
np:hasAssertion
dgn-np:NP854817.RAMkpO-Ov4CpyUSBIwxz1LhnNqgn3cwn9dS62t9KTVXSc130_assertion
;
np:hasProvenance
dgn-np:NP854817.RAMkpO-Ov4CpyUSBIwxz1LhnNqgn3cwn9dS62t9KTVXSc130_provenance
;
np:hasPublicationInfo
dgn-np:NP854817.RAMkpO-Ov4CpyUSBIwxz1LhnNqgn3cwn9dS62t9KTVXSc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP854817.RAMkpO-Ov4CpyUSBIwxz1LhnNqgn3cwn9dS62t9KTVXSc130_assertion
a
np:Assertion
.
dgn-np:NP854817.RAMkpO-Ov4CpyUSBIwxz1LhnNqgn3cwn9dS62t9KTVXSc130_provenance
a
np:Provenance
.
dgn-np:NP854817.RAMkpO-Ov4CpyUSBIwxz1LhnNqgn3cwn9dS62t9KTVXSc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP854817.RAMkpO-Ov4CpyUSBIwxz1LhnNqgn3cwn9dS62t9KTVXSc130_assertion
{
miriam-gene:270
a
ncit:C16612
.
lld:C0018802
a
ncit:C7057
.
dgn-gda:DGN18f210ba98cf296f78524f5576889478
sio:SIO_000628
miriam-gene:270
,
lld:C0018802
;
a
sio:SIO_001122
.
}
dgn-np:NP854817.RAMkpO-Ov4CpyUSBIwxz1LhnNqgn3cwn9dS62t9KTVXSc130_provenance
{
dgn-np:NP854817.RAMkpO-Ov4CpyUSBIwxz1LhnNqgn3cwn9dS62t9KTVXSc130_assertion
dcterms:description
"[AMPD1 C34T nonsense mutation is associated with reduced prevalence of diabetes and obesity in patients with CAD or HF, but A860T substitution seems to exert opposite metabolic effects and should always be accounted for in the studies of the AMPD1 genotype.]. 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:21108053
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP854817.RAMkpO-Ov4CpyUSBIwxz1LhnNqgn3cwn9dS62t9KTVXSc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:12+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}