@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y
> .
@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:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_head
{
this:
np:hasAssertion
dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_assertion
;
np:hasProvenance
dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_assertion
a
np:Assertion
.
dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_provenance
a
np:Provenance
.
dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_assertion
{
miriam-gene:7356
a
ncit:C16612
.
lld:C0017661
a
ncit:C7057
.
dgn-gda:DGNbdb6c6f3ddc5f83a186d59c8ac5644d8
sio:SIO_000628
miriam-gene:7356
,
lld:C0017661
;
a
sio:SIO_001122
.
}
dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_provenance
{
dgn-np:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_assertion
dcterms:description
"[The effect of G38A may be apparent under stimulation as sex steroids or infections, and homozygotes of the G38A mutation cannot produce sufficient UG in response to stimulation and may be predisposed to IgA nephropathy, especially in childhood.]. 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:11774099
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP147430.RAARMa2KcFaD2RwJ7aqrM-PLwLMJ1IJTCeQv7aHhfr18Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:17+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" .
}