@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP586660.RAWD6L_M8OXvokB7fYkyHbgdewuuyu3sosvx4jvCO2QWw
> .
@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:NP586660.RAWD6L_M8OXvokB7fYkyHbgdewuuyu3sosvx4jvCO2QWw130_head
{
this:
np:hasAssertion
dgn-np:NP586660.RAWD6L_M8OXvokB7fYkyHbgdewuuyu3sosvx4jvCO2QWw130_assertion
;
np:hasProvenance
dgn-np:NP586660.RAWD6L_M8OXvokB7fYkyHbgdewuuyu3sosvx4jvCO2QWw130_provenance
;
np:hasPublicationInfo
dgn-np:NP586660.RAWD6L_M8OXvokB7fYkyHbgdewuuyu3sosvx4jvCO2QWw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP586660.RAWD6L_M8OXvokB7fYkyHbgdewuuyu3sosvx4jvCO2QWw130_assertion
a
np:Assertion
.
dgn-np:NP586660.RAWD6L_M8OXvokB7fYkyHbgdewuuyu3sosvx4jvCO2QWw130_provenance
a
np:Provenance
.
dgn-np:NP586660.RAWD6L_M8OXvokB7fYkyHbgdewuuyu3sosvx4jvCO2QWw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP586660.RAWD6L_M8OXvokB7fYkyHbgdewuuyu3sosvx4jvCO2QWw130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0020501
a
ncit:C7057
.
dgn-gda:DGNfa9f9a94091c4608cf2719e268c2af2a
sio:SIO_000628
miriam-gene:183
,
lld:C0020501
;
a
sio:SIO_001121
.
}
dgn-np:NP586660.RAWD6L_M8OXvokB7fYkyHbgdewuuyu3sosvx4jvCO2QWw130_provenance
{
dgn-np:NP586660.RAWD6L_M8OXvokB7fYkyHbgdewuuyu3sosvx4jvCO2QWw130_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-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:NP586660.RAWD6L_M8OXvokB7fYkyHbgdewuuyu3sosvx4jvCO2QWw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}