@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8
> .
@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:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_head
{
this:
np:hasAssertion
dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_assertion
;
np:hasProvenance
dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_provenance
;
np:hasPublicationInfo
dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_assertion
a
np:Assertion
.
dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_provenance
a
np:Provenance
.
dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_assertion
{
miriam-gene:383
a
ncit:C16612
.
lld:C0026838
a
ncit:C7057
.
dgn-gda:DGN590d81a86944237aea314ae9edf39ecf
sio:SIO_000628
miriam-gene:383
,
lld:C0026838
;
a
sio:SIO_001121
.
}
dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_provenance
{
dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_assertion
dcterms:description
"[Since the spasticity and paucity of hyperammonemic crises seen in human AI-deficient patients are not features of the other urea cycle disorders, the likelihood of ammonia as the main neuropathogenic agent becomes extremely low, and the modest elevations of arginine seen in the brains of our mouse model of hyperargininemia make it an unlikely candidate as well.]. 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:17997338
;
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:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:05+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" .
}