@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP52326.RAjcqhOucAkhUqRrwBRBkqZ6uh65tD0XDPlnT1XQnYx2g
> .
@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:NP52326.RAjcqhOucAkhUqRrwBRBkqZ6uh65tD0XDPlnT1XQnYx2g130_head
{
this:
np:hasAssertion
dgn-np:NP52326.RAjcqhOucAkhUqRrwBRBkqZ6uh65tD0XDPlnT1XQnYx2g130_assertion
;
np:hasProvenance
dgn-np:NP52326.RAjcqhOucAkhUqRrwBRBkqZ6uh65tD0XDPlnT1XQnYx2g130_provenance
;
np:hasPublicationInfo
dgn-np:NP52326.RAjcqhOucAkhUqRrwBRBkqZ6uh65tD0XDPlnT1XQnYx2g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP52326.RAjcqhOucAkhUqRrwBRBkqZ6uh65tD0XDPlnT1XQnYx2g130_assertion
a
np:Assertion
.
dgn-np:NP52326.RAjcqhOucAkhUqRrwBRBkqZ6uh65tD0XDPlnT1XQnYx2g130_provenance
a
np:Provenance
.
dgn-np:NP52326.RAjcqhOucAkhUqRrwBRBkqZ6uh65tD0XDPlnT1XQnYx2g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP52326.RAjcqhOucAkhUqRrwBRBkqZ6uh65tD0XDPlnT1XQnYx2g130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN1a6340a856971f4604c40b4456dbfb54
sio:SIO_000628
miriam-gene:5972
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP52326.RAjcqhOucAkhUqRrwBRBkqZ6uh65tD0XDPlnT1XQnYx2g130_provenance
{
dgn-np:NP52326.RAjcqhOucAkhUqRrwBRBkqZ6uh65tD0XDPlnT1XQnYx2g130_assertion
dcterms:description
"[The results are evidence of similarities and some definite differences in genetic nature of the different forms of low-renin AH and, to say more widely, argue that the investigation of genetic predisposition for clinically heterogeneous forms of polygene diseases by comparison of groups of patients, separated in accordance with peculiarities of disease course, holds much promise for their hereditary background understanding.]. 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:18856058
;
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:NP52326.RAjcqhOucAkhUqRrwBRBkqZ6uh65tD0XDPlnT1XQnYx2g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}