@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP50078.RAEs8oST6nRcrvkOWehd4lFe6hTXtd9amzCp26fIFPr1k
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP50078.RAEs8oST6nRcrvkOWehd4lFe6hTXtd9amzCp26fIFPr1k130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP50078.RAEs8oST6nRcrvkOWehd4lFe6hTXtd9amzCp26fIFPr1k130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP50078.RAEs8oST6nRcrvkOWehd4lFe6hTXtd9amzCp26fIFPr1k130_assertion
a
np:Assertion
.
dgn-np:NP50078.RAEs8oST6nRcrvkOWehd4lFe6hTXtd9amzCp26fIFPr1k130_provenance
a
np:Provenance
.
dgn-np:NP50078.RAEs8oST6nRcrvkOWehd4lFe6hTXtd9amzCp26fIFPr1k130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:7124
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN869f1c1b081e93caad64c99abfd2c2e3
sio:SIO_000628
miriam-gene:7124
,
lld:C0020538
;
a
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.
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dgn-np:NP50078.RAEs8oST6nRcrvkOWehd4lFe6hTXtd9amzCp26fIFPr1k130_provenance
{
dgn-np:NP50078.RAEs8oST6nRcrvkOWehd4lFe6hTXtd9amzCp26fIFPr1k130_assertion
dcterms:description
"[However, although they do not reach statistical significance (which may be due to the relatively restricted number of subjects included in this study), the distribution differences (in normotensives and hypertensives) observed in the cases of EGF and TNF-alpha reflect trends that could be expected from a mechanistic explanation of the pathways that underlie the patho-physiology of hypertension.]. 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:12009575
;
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 .
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dgn-np:NP50078.RAEs8oST6nRcrvkOWehd4lFe6hTXtd9amzCp26fIFPr1k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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
<
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> , <
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
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