@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP508310.RAf1XmQ4fD1u6I4chqUs6b9mLPt_7ZdRZlPVeWfHfvbbA
> .
@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:NP508310.RAf1XmQ4fD1u6I4chqUs6b9mLPt_7ZdRZlPVeWfHfvbbA130_head
{
this:
np:hasAssertion
dgn-np:NP508310.RAf1XmQ4fD1u6I4chqUs6b9mLPt_7ZdRZlPVeWfHfvbbA130_assertion
;
np:hasProvenance
dgn-np:NP508310.RAf1XmQ4fD1u6I4chqUs6b9mLPt_7ZdRZlPVeWfHfvbbA130_provenance
;
np:hasPublicationInfo
dgn-np:NP508310.RAf1XmQ4fD1u6I4chqUs6b9mLPt_7ZdRZlPVeWfHfvbbA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP508310.RAf1XmQ4fD1u6I4chqUs6b9mLPt_7ZdRZlPVeWfHfvbbA130_assertion
a
np:Assertion
.
dgn-np:NP508310.RAf1XmQ4fD1u6I4chqUs6b9mLPt_7ZdRZlPVeWfHfvbbA130_provenance
a
np:Provenance
.
dgn-np:NP508310.RAf1XmQ4fD1u6I4chqUs6b9mLPt_7ZdRZlPVeWfHfvbbA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP508310.RAf1XmQ4fD1u6I4chqUs6b9mLPt_7ZdRZlPVeWfHfvbbA130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0018799
a
ncit:C7057
.
dgn-gda:DGNa55decf86332fb5a8e48b51abf6ee0b4
sio:SIO_000628
miriam-gene:1636
,
lld:C0018799
;
a
sio:SIO_001121
.
}
dgn-np:NP508310.RAf1XmQ4fD1u6I4chqUs6b9mLPt_7ZdRZlPVeWfHfvbbA130_provenance
{
dgn-np:NP508310.RAf1XmQ4fD1u6I4chqUs6b9mLPt_7ZdRZlPVeWfHfvbbA130_assertion
dcterms:description
"[A simplified DNA extraction protocol coupled to the high throughput capability of the MADGE electrophoretic system for genotyping enables analysis of large populations for association studies of ACE genotype with cardiac disease events.]. 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:7756072
;
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:NP508310.RAf1XmQ4fD1u6I4chqUs6b9mLPt_7ZdRZlPVeWfHfvbbA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:03+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" .
}