@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo
> .
@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:NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_head
{
this:
np:hasAssertion
dgn-np:NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_assertion
;
np:hasProvenance
dgn-np:NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_provenance
;
np:hasPublicationInfo
dgn-np:NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_assertion
a
np:Assertion
.
dgn-np:NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_provenance
a
np:Provenance
.
dgn-np:NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_assertion
{
miriam-gene:1906
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGN3f1dc62b7dc5d8ad1e008f68a418d4fb
sio:SIO_000628
miriam-gene:1906
,
lld:C0022658
;
a
sio:SIO_001122
.
}
dgn-np:NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_provenance
{
dgn-np:NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_assertion
dcterms:description
"[Moreover, the frequency of endothelin-1 Lys198Asn polymorphism was investigated with respect to the prevalence of several actual or historical endorgan damages (renal disorder, coronary artery disease, vascular events, vascular damage, and congestive heart failure) in hypertensive patients.]. 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:18923236
;
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:NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:01+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" .
}