@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP977367.RAJ31W1AMiBLDQHJMURl-8srAMv3bcvr_rUMt7KJs0rnQ
> .
@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/v3.0.0/void/
> .
dgn-np:NP977367.RAJ31W1AMiBLDQHJMURl-8srAMv3bcvr_rUMt7KJs0rnQ130_head
{
this:
np:hasAssertion
dgn-np:NP977367.RAJ31W1AMiBLDQHJMURl-8srAMv3bcvr_rUMt7KJs0rnQ130_assertion
;
np:hasProvenance
dgn-np:NP977367.RAJ31W1AMiBLDQHJMURl-8srAMv3bcvr_rUMt7KJs0rnQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP977367.RAJ31W1AMiBLDQHJMURl-8srAMv3bcvr_rUMt7KJs0rnQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP977367.RAJ31W1AMiBLDQHJMURl-8srAMv3bcvr_rUMt7KJs0rnQ130_assertion
a
np:Assertion
.
dgn-np:NP977367.RAJ31W1AMiBLDQHJMURl-8srAMv3bcvr_rUMt7KJs0rnQ130_provenance
a
np:Provenance
.
dgn-np:NP977367.RAJ31W1AMiBLDQHJMURl-8srAMv3bcvr_rUMt7KJs0rnQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP977367.RAJ31W1AMiBLDQHJMURl-8srAMv3bcvr_rUMt7KJs0rnQ130_assertion
{
miriam-gene:162417
a
ncit:C16612
.
lld:C0268543
a
ncit:C7057
.
dgn-gda:DGN82b3dfad84eeb85898cd6de0917da39c
sio:SIO_000628
miriam-gene:162417
,
lld:C0268543
;
a
sio:SIO_001121
.
}
dgn-np:NP977367.RAJ31W1AMiBLDQHJMURl-8srAMv3bcvr_rUMt7KJs0rnQ130_provenance
{
dgn-np:NP977367.RAJ31W1AMiBLDQHJMURl-8srAMv3bcvr_rUMt7KJs0rnQ130_assertion
dcterms:description
"[NAGS deficiency in humans leads to hyperammonemia and can be primary, due to mutations in the NAGS gene or secondary due to other mitochondrial aberrations that interfere with the normal function of the same enzyme.]. 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:20303810
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP977367.RAJ31W1AMiBLDQHJMURl-8srAMv3bcvr_rUMt7KJs0rnQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:37+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}