@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP485891.RAtZ_I5nnJuUvtULq1OgV4SN1bxBEy3qwXzLTNb6hmiYU
> .
@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:NP485891.RAtZ_I5nnJuUvtULq1OgV4SN1bxBEy3qwXzLTNb6hmiYU130_head
{
this:
np:hasAssertion
dgn-np:NP485891.RAtZ_I5nnJuUvtULq1OgV4SN1bxBEy3qwXzLTNb6hmiYU130_assertion
;
np:hasProvenance
dgn-np:NP485891.RAtZ_I5nnJuUvtULq1OgV4SN1bxBEy3qwXzLTNb6hmiYU130_provenance
;
np:hasPublicationInfo
dgn-np:NP485891.RAtZ_I5nnJuUvtULq1OgV4SN1bxBEy3qwXzLTNb6hmiYU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP485891.RAtZ_I5nnJuUvtULq1OgV4SN1bxBEy3qwXzLTNb6hmiYU130_assertion
a
np:Assertion
.
dgn-np:NP485891.RAtZ_I5nnJuUvtULq1OgV4SN1bxBEy3qwXzLTNb6hmiYU130_provenance
a
np:Provenance
.
dgn-np:NP485891.RAtZ_I5nnJuUvtULq1OgV4SN1bxBEy3qwXzLTNb6hmiYU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP485891.RAtZ_I5nnJuUvtULq1OgV4SN1bxBEy3qwXzLTNb6hmiYU130_assertion
{
miriam-gene:59272
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN98c359d8cc943abff4f131419d0ffca2
sio:SIO_000628
miriam-gene:59272
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP485891.RAtZ_I5nnJuUvtULq1OgV4SN1bxBEy3qwXzLTNb6hmiYU130_provenance
{
dgn-np:NP485891.RAtZ_I5nnJuUvtULq1OgV4SN1bxBEy3qwXzLTNb6hmiYU130_assertion
dcterms:description
"[The ACE2 gene maps to chromosome Xp22 and this paper reviews the evidence associating ACE2 gene variation with CVD and considers clues to potential functional ACE2 variants that may alter gene expression or transcriptional activity.]. 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:23013041
;
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:NP485891.RAtZ_I5nnJuUvtULq1OgV4SN1bxBEy3qwXzLTNb6hmiYU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}