@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w
> .
@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:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_head
{
this:
np:hasAssertion
dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_assertion
;
np:hasProvenance
dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_provenance
;
np:hasPublicationInfo
dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_assertion
a
np:Assertion
.
dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_provenance
a
np:Provenance
.
dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_assertion
{
miriam-gene:5444
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN1ce2fbad7c5395a65f9012b7ab1bd945
sio:SIO_000628
miriam-gene:5444
,
lld:C0004153
;
a
sio:SIO_001122
.
}
dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_provenance
{
dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_assertion
dcterms:description
"[A common polymorphism in the PON gene (PON1) causes an amino acid substitution of methionine (M) for leucine (L) at position 55 in the protein, which changes the activity of PON and can affect the risk of atherosclerosis.]. 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:11555845
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}