@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP752189.RAIeZ32YH_0a9xmEu7iUeoNPb2Imwt5P7Pe2wv2eljlBw
> .
@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:NP752189.RAIeZ32YH_0a9xmEu7iUeoNPb2Imwt5P7Pe2wv2eljlBw130_head
{
this:
np:hasAssertion
dgn-np:NP752189.RAIeZ32YH_0a9xmEu7iUeoNPb2Imwt5P7Pe2wv2eljlBw130_assertion
;
np:hasProvenance
dgn-np:NP752189.RAIeZ32YH_0a9xmEu7iUeoNPb2Imwt5P7Pe2wv2eljlBw130_provenance
;
np:hasPublicationInfo
dgn-np:NP752189.RAIeZ32YH_0a9xmEu7iUeoNPb2Imwt5P7Pe2wv2eljlBw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP752189.RAIeZ32YH_0a9xmEu7iUeoNPb2Imwt5P7Pe2wv2eljlBw130_assertion
a
np:Assertion
.
dgn-np:NP752189.RAIeZ32YH_0a9xmEu7iUeoNPb2Imwt5P7Pe2wv2eljlBw130_provenance
a
np:Provenance
.
dgn-np:NP752189.RAIeZ32YH_0a9xmEu7iUeoNPb2Imwt5P7Pe2wv2eljlBw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP752189.RAIeZ32YH_0a9xmEu7iUeoNPb2Imwt5P7Pe2wv2eljlBw130_assertion
{
miriam-gene:189
a
ncit:C16612
.
lld:C0020501
a
ncit:C7057
.
dgn-gda:DGN5b66b9f89fd1df3a47c6a68b0934890a
sio:SIO_000628
miriam-gene:189
,
lld:C0020501
;
a
sio:SIO_001121
.
}
dgn-np:NP752189.RAIeZ32YH_0a9xmEu7iUeoNPb2Imwt5P7Pe2wv2eljlBw130_provenance
{
dgn-np:NP752189.RAIeZ32YH_0a9xmEu7iUeoNPb2Imwt5P7Pe2wv2eljlBw130_assertion
dcterms:description
"[These results are discussed with reference to the AGT targeting defect in primary hyperoxaluria and also in relation to the highly unusual species specificity of subcellular distribution of AGT among mammals.]. 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:1961759
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP752189.RAIeZ32YH_0a9xmEu7iUeoNPb2Imwt5P7Pe2wv2eljlBw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:26+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" .
}