@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP148206.RAf9d8AuIm1TAEtBqSDZiXC0YO6lc60ptqRZ_xIQuJWx4
> .
@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:NP148206.RAf9d8AuIm1TAEtBqSDZiXC0YO6lc60ptqRZ_xIQuJWx4130_head
{
this:
np:hasAssertion
dgn-np:NP148206.RAf9d8AuIm1TAEtBqSDZiXC0YO6lc60ptqRZ_xIQuJWx4130_assertion
;
np:hasProvenance
dgn-np:NP148206.RAf9d8AuIm1TAEtBqSDZiXC0YO6lc60ptqRZ_xIQuJWx4130_provenance
;
np:hasPublicationInfo
dgn-np:NP148206.RAf9d8AuIm1TAEtBqSDZiXC0YO6lc60ptqRZ_xIQuJWx4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP148206.RAf9d8AuIm1TAEtBqSDZiXC0YO6lc60ptqRZ_xIQuJWx4130_assertion
a
np:Assertion
.
dgn-np:NP148206.RAf9d8AuIm1TAEtBqSDZiXC0YO6lc60ptqRZ_xIQuJWx4130_provenance
a
np:Provenance
.
dgn-np:NP148206.RAf9d8AuIm1TAEtBqSDZiXC0YO6lc60ptqRZ_xIQuJWx4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP148206.RAf9d8AuIm1TAEtBqSDZiXC0YO6lc60ptqRZ_xIQuJWx4130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0007785
a
ncit:C7057
.
dgn-gda:DGN7882f86ed57c841a7ad7097a9b3a5fe0
sio:SIO_000628
miriam-gene:183
,
lld:C0007785
;
a
sio:SIO_001122
.
}
dgn-np:NP148206.RAf9d8AuIm1TAEtBqSDZiXC0YO6lc60ptqRZ_xIQuJWx4130_provenance
{
dgn-np:NP148206.RAf9d8AuIm1TAEtBqSDZiXC0YO6lc60ptqRZ_xIQuJWx4130_assertion
dcterms:description
"[single nucleotide polymorphism (SNP) haplotypes may play an important role in pathogenesis of primary hypertension and be the genetic risk factors for the onset of primary hypertension with 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:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP148206.RAf9d8AuIm1TAEtBqSDZiXC0YO6lc60ptqRZ_xIQuJWx4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:17+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" .
}