@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix ns1: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1412562.RA_DJBHecN8VrkN0amGFBV-JtDxFtODiSK_4daDRJ87So
> .
@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 np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
ns1:NP1412562.RA_DJBHecN8VrkN0amGFBV-JtDxFtODiSK_4daDRJ87So130_head
{
this:
np:hasAssertion
ns1:NP1412562.RA_DJBHecN8VrkN0amGFBV-JtDxFtODiSK_4daDRJ87So130_assertion
;
np:hasProvenance
ns1:NP1412562.RA_DJBHecN8VrkN0amGFBV-JtDxFtODiSK_4daDRJ87So130_provenance
;
np:hasPublicationInfo
ns1:NP1412562.RA_DJBHecN8VrkN0amGFBV-JtDxFtODiSK_4daDRJ87So130_publicationInfo
;
a
np:Nanopublication
.
ns1:NP1412562.RA_DJBHecN8VrkN0amGFBV-JtDxFtODiSK_4daDRJ87So130_assertion
a
np:Assertion
.
ns1:NP1412562.RA_DJBHecN8VrkN0amGFBV-JtDxFtODiSK_4daDRJ87So130_provenance
a
np:Provenance
.
ns1:NP1412562.RA_DJBHecN8VrkN0amGFBV-JtDxFtODiSK_4daDRJ87So130_publicationInfo
a
np:PublicationInfo
.
}
ns1:NP1412562.RA_DJBHecN8VrkN0amGFBV-JtDxFtODiSK_4daDRJ87So130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN684cad4e14b369a5d6fde61c32795621
sio:SIO_000628
miriam-gene:1636
,
lld:C0020538
;
a
sio:SIO_001121
.
}
ns1:NP1412562.RA_DJBHecN8VrkN0amGFBV-JtDxFtODiSK_4daDRJ87So130_provenance
{
ns1:NP1412562.RA_DJBHecN8VrkN0amGFBV-JtDxFtODiSK_4daDRJ87So130_assertion
dct:description
"[A variant in the angiotensin-converting enzyme gene could not, initially, be convincingly associated with hypertension, but more recent analyses suggest an influence of the deletion allele on blood pressure in men, but apparently not in women.]. 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:9886871
;
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 .
}
ns1:NP1412562.RA_DJBHecN8VrkN0amGFBV-JtDxFtODiSK_4daDRJ87So130_publicationInfo
{
this:
dct:created
"2016-05-13T12:52:27+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct: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" .
}