@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP185431.RAulOe9Ea0ZTbxbIClwWDGyHHXHbnanTBq_LRMw9ScbhA
> .
@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:NP185431.RAulOe9Ea0ZTbxbIClwWDGyHHXHbnanTBq_LRMw9ScbhA130_head
{
this:
np:hasAssertion
dgn-np:NP185431.RAulOe9Ea0ZTbxbIClwWDGyHHXHbnanTBq_LRMw9ScbhA130_assertion
;
np:hasProvenance
dgn-np:NP185431.RAulOe9Ea0ZTbxbIClwWDGyHHXHbnanTBq_LRMw9ScbhA130_provenance
;
np:hasPublicationInfo
dgn-np:NP185431.RAulOe9Ea0ZTbxbIClwWDGyHHXHbnanTBq_LRMw9ScbhA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP185431.RAulOe9Ea0ZTbxbIClwWDGyHHXHbnanTBq_LRMw9ScbhA130_assertion
a
np:Assertion
.
dgn-np:NP185431.RAulOe9Ea0ZTbxbIClwWDGyHHXHbnanTBq_LRMw9ScbhA130_provenance
a
np:Provenance
.
dgn-np:NP185431.RAulOe9Ea0ZTbxbIClwWDGyHHXHbnanTBq_LRMw9ScbhA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP185431.RAulOe9Ea0ZTbxbIClwWDGyHHXHbnanTBq_LRMw9ScbhA130_assertion
{
miriam-gene:2821
a
ncit:C16612
.
lld:C0002878
a
ncit:C7057
.
dgn-gda:DGNc817c3b10aa0fe8842aca55be9ce9ab8
sio:SIO_000628
miriam-gene:2821
,
lld:C0002878
;
a
sio:SIO_001121
.
}
dgn-np:NP185431.RAulOe9Ea0ZTbxbIClwWDGyHHXHbnanTBq_LRMw9ScbhA130_provenance
{
dgn-np:NP185431.RAulOe9Ea0ZTbxbIClwWDGyHHXHbnanTBq_LRMw9ScbhA130_assertion
dcterms:description
"[The pathogenesis of two metabolic disorders caused by enzyme defects in the red blood cell leading to hemolytic anemia, and in some cases of glucose phosphate isomerase (GPI) deficiency additionally to neurological impairment was investigated.]. 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:9362562
;
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:NP185431.RAulOe9Ea0ZTbxbIClwWDGyHHXHbnanTBq_LRMw9ScbhA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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" .
}