@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP70418.RANYdCvtXNG_ZGOIoIswSarnfqEQUlzG3KMqcgHg5yqCQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP70418.RANYdCvtXNG_ZGOIoIswSarnfqEQUlzG3KMqcgHg5yqCQ130_head
{
this:
np:hasAssertion
dgn-np:NP70418.RANYdCvtXNG_ZGOIoIswSarnfqEQUlzG3KMqcgHg5yqCQ130_assertion
;
np:hasProvenance
dgn-np:NP70418.RANYdCvtXNG_ZGOIoIswSarnfqEQUlzG3KMqcgHg5yqCQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP70418.RANYdCvtXNG_ZGOIoIswSarnfqEQUlzG3KMqcgHg5yqCQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP70418.RANYdCvtXNG_ZGOIoIswSarnfqEQUlzG3KMqcgHg5yqCQ130_assertion
a
np:Assertion
.
dgn-np:NP70418.RANYdCvtXNG_ZGOIoIswSarnfqEQUlzG3KMqcgHg5yqCQ130_provenance
a
np:Provenance
.
dgn-np:NP70418.RANYdCvtXNG_ZGOIoIswSarnfqEQUlzG3KMqcgHg5yqCQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP70418.RANYdCvtXNG_ZGOIoIswSarnfqEQUlzG3KMqcgHg5yqCQ130_assertion
{
miriam-gene:4878
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN457ccb74fd5e273761b3a6594439f427
sio:SIO_000628
miriam-gene:4878
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP70418.RANYdCvtXNG_ZGOIoIswSarnfqEQUlzG3KMqcgHg5yqCQ130_provenance
{
dgn-np:NP70418.RANYdCvtXNG_ZGOIoIswSarnfqEQUlzG3KMqcgHg5yqCQ130_assertion
dcterms:description
"[We conclude that the mutated genotypes of the ScaI polymorphism are negatively associated with overt nephropathy, whereas the mutated genotypes of BstXI polymorphism are positively associated with microalbuminuria. hANP gene variants may exert a protecti]. 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:11408388
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP70418.RANYdCvtXNG_ZGOIoIswSarnfqEQUlzG3KMqcgHg5yqCQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:20+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}