@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM
> .
@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:NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130_head
{
this:
np:hasAssertion
dgn-np:NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130_assertion
;
np:hasProvenance
dgn-np:NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130_provenance
;
np:hasPublicationInfo
dgn-np:NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130_assertion
a
np:Assertion
.
dgn-np:NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130_provenance
a
np:Provenance
.
dgn-np:NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130_assertion
{
miriam-gene:3816
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNdb235e24749c6842804d44bea04bccaf
sio:SIO_000628
miriam-gene:3816
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130_provenance
{
dgn-np:NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130_assertion
dcterms:description
"[In conclusion, there are polymorphisms in the regulatory region of human tissue kallikrein gene in the Chinese Han people. Differences in both allele frequencies and genotype frequencies between these two groups have provided evidence towards the association of hypertension with the polymorphisms in this studied site.]. 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:15905889
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP55513.RAZv3OcMA7REU4Ol3HOVu9cdziVKeaAZf3B7rByDVu7NM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:26+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" .
}