@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP560668.RAZf-3BfmK6R4adr-z8cGONMh1RFISKV_28AdcXen1mkk
> .
@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:NP560668.RAZf-3BfmK6R4adr-z8cGONMh1RFISKV_28AdcXen1mkk130_head
{
this:
np:hasAssertion
dgn-np:NP560668.RAZf-3BfmK6R4adr-z8cGONMh1RFISKV_28AdcXen1mkk130_assertion
;
np:hasProvenance
dgn-np:NP560668.RAZf-3BfmK6R4adr-z8cGONMh1RFISKV_28AdcXen1mkk130_provenance
;
np:hasPublicationInfo
dgn-np:NP560668.RAZf-3BfmK6R4adr-z8cGONMh1RFISKV_28AdcXen1mkk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP560668.RAZf-3BfmK6R4adr-z8cGONMh1RFISKV_28AdcXen1mkk130_assertion
a
np:Assertion
.
dgn-np:NP560668.RAZf-3BfmK6R4adr-z8cGONMh1RFISKV_28AdcXen1mkk130_provenance
a
np:Provenance
.
dgn-np:NP560668.RAZf-3BfmK6R4adr-z8cGONMh1RFISKV_28AdcXen1mkk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP560668.RAZf-3BfmK6R4adr-z8cGONMh1RFISKV_28AdcXen1mkk130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN3bb2c9d018bb22bdc5b81ad5c0389e2e
sio:SIO_000628
miriam-gene:183
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP560668.RAZf-3BfmK6R4adr-z8cGONMh1RFISKV_28AdcXen1mkk130_provenance
{
dgn-np:NP560668.RAZf-3BfmK6R4adr-z8cGONMh1RFISKV_28AdcXen1mkk130_assertion
dcterms:description
"[To investigate the relationship of four single nucleotide polymorphism (SNP) haplotypes in the angiotensinogen (AGT) gene to the primary hypertension with or without cerebral infarction in the Li nationality of Hainan, China.]. 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:17952138
;
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:NP560668.RAZf-3BfmK6R4adr-z8cGONMh1RFISKV_28AdcXen1mkk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}