@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP687636.RAbWmxQ_VfCRkJFitYpoVZziBBWjbNLpw7Wk1hYKPdrvc
> .
@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:NP687636.RAbWmxQ_VfCRkJFitYpoVZziBBWjbNLpw7Wk1hYKPdrvc130_head
{
this:
np:hasAssertion
dgn-np:NP687636.RAbWmxQ_VfCRkJFitYpoVZziBBWjbNLpw7Wk1hYKPdrvc130_assertion
;
np:hasProvenance
dgn-np:NP687636.RAbWmxQ_VfCRkJFitYpoVZziBBWjbNLpw7Wk1hYKPdrvc130_provenance
;
np:hasPublicationInfo
dgn-np:NP687636.RAbWmxQ_VfCRkJFitYpoVZziBBWjbNLpw7Wk1hYKPdrvc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP687636.RAbWmxQ_VfCRkJFitYpoVZziBBWjbNLpw7Wk1hYKPdrvc130_assertion
a
np:Assertion
.
dgn-np:NP687636.RAbWmxQ_VfCRkJFitYpoVZziBBWjbNLpw7Wk1hYKPdrvc130_provenance
a
np:Provenance
.
dgn-np:NP687636.RAbWmxQ_VfCRkJFitYpoVZziBBWjbNLpw7Wk1hYKPdrvc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP687636.RAbWmxQ_VfCRkJFitYpoVZziBBWjbNLpw7Wk1hYKPdrvc130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0730345
a
ncit:C7057
.
dgn-gda:DGNa9a97a29e1bab2ece9c0c8087de94815
sio:SIO_000628
miriam-gene:183
,
lld:C0730345
;
a
sio:SIO_001121
.
}
dgn-np:NP687636.RAbWmxQ_VfCRkJFitYpoVZziBBWjbNLpw7Wk1hYKPdrvc130_provenance
{
dgn-np:NP687636.RAbWmxQ_VfCRkJFitYpoVZziBBWjbNLpw7Wk1hYKPdrvc130_assertion
dcterms:description
"[Regression analysis confirmed negative (AMM) and positive (GTM, ATT, GMT, AMT) association of AGT haplotypes with microalbuminuria, and negative (AMM) and positive (GTM and ATT) association of AGT haplotypes with macroalbuminuria.]. 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:21421655
;
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:NP687636.RAbWmxQ_VfCRkJFitYpoVZziBBWjbNLpw7Wk1hYKPdrvc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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" .
}