@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg
> .
@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:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_head
{
this:
np:hasAssertion
dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_assertion
;
np:hasProvenance
dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_provenance
;
np:hasPublicationInfo
dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_assertion
a
np:Assertion
.
dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_provenance
a
np:Provenance
.
dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_assertion
{
miriam-gene:57379
a
ncit:C16612
.
lld:C1306589
a
ncit:C7057
.
dgn-gda:DGN3d6236cf14effa9d550eb9de742a48e7
sio:SIO_000628
miriam-gene:57379
,
lld:C1306589
;
a
sio:SIO_001121
.
}
dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_provenance
{
dgn-np:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_assertion
dcterms:description
"[After the identification of the locus for CDA II, also known as HEMPAS (hereditary erythroblast multinuclearity with positive acidified serum test), on the long arm of chromosome 20 (20q11.2) we have analyzed by a mutational search seven candidate genes in a large series of CDA II patients.]. 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:12667984
;
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:NP290734.RAH78uf9ipXVxvaSCKNq-R0eq3tGLDEPF-UQUaejOfHTg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:45+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" .
}