@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM
> .
@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:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_head
{
this:
np:hasAssertion
dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_assertion
;
np:hasProvenance
dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_provenance
;
np:hasPublicationInfo
dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_assertion
a
np:Assertion
.
dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_provenance
a
np:Provenance
.
dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_assertion
{
miriam-gene:23038
a
ncit:C16612
.
lld:C1863239
a
ncit:C7057
.
dgn-gda:DGNcccaa0ae89030e2072712af8c1f630e0
sio:SIO_000628
miriam-gene:23038
,
lld:C1863239
;
a
sio:SIO_001121
.
}
dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_provenance
{
dgn-np:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_assertion
dcterms:description
"[Excessive poly(ADP-ribose) synthesis, provoked by DNA strand breakage, may represent a common pathway that connects the immunodeficiency syndromes associated with (a) exposure of lymphocytes to toxic oxygen species during chronic inflammatory states, (b) adenosine deaminase deficiency, and (c) certain DNA repair disorders.]. 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:3950545
;
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:NP448903.RA1eM3eBh60IzYJskkGFgqNT2LaZw0ELkDopSFSbzbyWM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:28+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" .
}