@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP887999.RAQigLYLvi5HOHVKg0K0_KcLxtEQGrm3XJxTPRijqc61Q
> .
@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:NP887999.RAQigLYLvi5HOHVKg0K0_KcLxtEQGrm3XJxTPRijqc61Q130_head
{
this:
np:hasAssertion
dgn-np:NP887999.RAQigLYLvi5HOHVKg0K0_KcLxtEQGrm3XJxTPRijqc61Q130_assertion
;
np:hasProvenance
dgn-np:NP887999.RAQigLYLvi5HOHVKg0K0_KcLxtEQGrm3XJxTPRijqc61Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP887999.RAQigLYLvi5HOHVKg0K0_KcLxtEQGrm3XJxTPRijqc61Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP887999.RAQigLYLvi5HOHVKg0K0_KcLxtEQGrm3XJxTPRijqc61Q130_assertion
a
np:Assertion
.
dgn-np:NP887999.RAQigLYLvi5HOHVKg0K0_KcLxtEQGrm3XJxTPRijqc61Q130_provenance
a
np:Provenance
.
dgn-np:NP887999.RAQigLYLvi5HOHVKg0K0_KcLxtEQGrm3XJxTPRijqc61Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP887999.RAQigLYLvi5HOHVKg0K0_KcLxtEQGrm3XJxTPRijqc61Q130_assertion
{
miriam-gene:1659
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNc424e122b44bf673e6dd2320fd23be0c
sio:SIO_000628
miriam-gene:1659
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP887999.RAQigLYLvi5HOHVKg0K0_KcLxtEQGrm3XJxTPRijqc61Q130_provenance
{
dgn-np:NP887999.RAQigLYLvi5HOHVKg0K0_KcLxtEQGrm3XJxTPRijqc61Q130_assertion
dcterms:description
"[We did not find any evidence of association of the two novel SNPs in MDM4 and HRH1 with sequelae of high BP including coronary artery disease (CAD), left ventricular hypertrophy (LVH) or stroke.]. 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:23303523
;
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:NP887999.RAQigLYLvi5HOHVKg0K0_KcLxtEQGrm3XJxTPRijqc61Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:05+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" .
}