@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP368635.RAqBWLsO8Dxwra4BA7zIm5X5-TM_8_gspwhoVW1ICoVNc
> .
@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:NP368635.RAqBWLsO8Dxwra4BA7zIm5X5-TM_8_gspwhoVW1ICoVNc130_head
{
this:
np:hasAssertion
dgn-np:NP368635.RAqBWLsO8Dxwra4BA7zIm5X5-TM_8_gspwhoVW1ICoVNc130_assertion
;
np:hasProvenance
dgn-np:NP368635.RAqBWLsO8Dxwra4BA7zIm5X5-TM_8_gspwhoVW1ICoVNc130_provenance
;
np:hasPublicationInfo
dgn-np:NP368635.RAqBWLsO8Dxwra4BA7zIm5X5-TM_8_gspwhoVW1ICoVNc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP368635.RAqBWLsO8Dxwra4BA7zIm5X5-TM_8_gspwhoVW1ICoVNc130_assertion
a
np:Assertion
.
dgn-np:NP368635.RAqBWLsO8Dxwra4BA7zIm5X5-TM_8_gspwhoVW1ICoVNc130_provenance
a
np:Provenance
.
dgn-np:NP368635.RAqBWLsO8Dxwra4BA7zIm5X5-TM_8_gspwhoVW1ICoVNc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP368635.RAqBWLsO8Dxwra4BA7zIm5X5-TM_8_gspwhoVW1ICoVNc130_assertion
{
miriam-gene:3643
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN82221ef0b945de2b52331643fd72e4c0
sio:SIO_000628
miriam-gene:3643
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP368635.RAqBWLsO8Dxwra4BA7zIm5X5-TM_8_gspwhoVW1ICoVNc130_provenance
{
dgn-np:NP368635.RAqBWLsO8Dxwra4BA7zIm5X5-TM_8_gspwhoVW1ICoVNc130_assertion
dcterms:description
"[All but one of the hypertensive subjects had at least one of the hypertension-associated alleles, and although subjects homozygous for both were three times more frequent in the hypertensive group, examination of the nine possible genotypes suggested that the INSR and DCP1 alleles are independent markers for 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:8104754
;
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:NP368635.RAqBWLsO8Dxwra4BA7zIm5X5-TM_8_gspwhoVW1ICoVNc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:35+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" .
}