@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY
> .
@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:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_head
{
this:
np:hasAssertion
dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_assertion
;
np:hasProvenance
dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_provenance
;
np:hasPublicationInfo
dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_assertion
a
np:Assertion
.
dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_provenance
a
np:Provenance
.
dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_assertion
{
miriam-gene:158
a
ncit:C16612
.
lld:C0268126
a
ncit:C7057
.
dgn-gda:DGN2b794d6cb547c7682d1fa3a246681b54
sio:SIO_000628
miriam-gene:158
,
lld:C0268126
;
a
sio:SIO_001121
.
}
dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_provenance
{
dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_assertion
dcterms:description
"[The results also corroborate the hypothesis that the phenotypic severity of ADSL deficiency is mainly determined by structural stability and residual catalytic capacity of the corresponding mutant ADSL protein complexes, as this is prerequisite for the formation and stability of the purinosome and at least partial channeling of succinylaminoimidazolecarboxamide riboside-ADSL enzyme substrates-through the DNPS pathway.]. 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:22180458
;
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:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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" .
}