@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP370416.RA8xewLGPKF3R4RnLk4xUP5Cz7RkAX7n1R_7neNktpVi8
> .
@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:NP370416.RA8xewLGPKF3R4RnLk4xUP5Cz7RkAX7n1R_7neNktpVi8130_head
{
this:
np:hasAssertion
dgn-np:NP370416.RA8xewLGPKF3R4RnLk4xUP5Cz7RkAX7n1R_7neNktpVi8130_assertion
;
np:hasProvenance
dgn-np:NP370416.RA8xewLGPKF3R4RnLk4xUP5Cz7RkAX7n1R_7neNktpVi8130_provenance
;
np:hasPublicationInfo
dgn-np:NP370416.RA8xewLGPKF3R4RnLk4xUP5Cz7RkAX7n1R_7neNktpVi8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP370416.RA8xewLGPKF3R4RnLk4xUP5Cz7RkAX7n1R_7neNktpVi8130_assertion
a
np:Assertion
.
dgn-np:NP370416.RA8xewLGPKF3R4RnLk4xUP5Cz7RkAX7n1R_7neNktpVi8130_provenance
a
np:Provenance
.
dgn-np:NP370416.RA8xewLGPKF3R4RnLk4xUP5Cz7RkAX7n1R_7neNktpVi8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP370416.RA8xewLGPKF3R4RnLk4xUP5Cz7RkAX7n1R_7neNktpVi8130_assertion
{
miriam-gene:7133
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNb999c847fd67720b04f34c140b0b393d
sio:SIO_000628
miriam-gene:7133
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP370416.RA8xewLGPKF3R4RnLk4xUP5Cz7RkAX7n1R_7neNktpVi8130_provenance
{
dgn-np:NP370416.RA8xewLGPKF3R4RnLk4xUP5Cz7RkAX7n1R_7neNktpVi8130_assertion
dcterms:description
"[The case-control study in 134 unrelated HTs who were the offspring of two HT parents and 197 normotensives (NTs) whose parents were both NTs, indicated possible association of TNFRSF1B with HT by haplotype analysis (P = 0.008).]. 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:10942422
;
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:NP370416.RA8xewLGPKF3R4RnLk4xUP5Cz7RkAX7n1R_7neNktpVi8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:37+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" .
}