@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP797602.RAgg_H4TXau2Wi8ZDwS6biyb71g96fusdkZJwzZyLbz4E
> .
@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:NP797602.RAgg_H4TXau2Wi8ZDwS6biyb71g96fusdkZJwzZyLbz4E130_head
{
this:
np:hasAssertion
dgn-np:NP797602.RAgg_H4TXau2Wi8ZDwS6biyb71g96fusdkZJwzZyLbz4E130_assertion
;
np:hasProvenance
dgn-np:NP797602.RAgg_H4TXau2Wi8ZDwS6biyb71g96fusdkZJwzZyLbz4E130_provenance
;
np:hasPublicationInfo
dgn-np:NP797602.RAgg_H4TXau2Wi8ZDwS6biyb71g96fusdkZJwzZyLbz4E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP797602.RAgg_H4TXau2Wi8ZDwS6biyb71g96fusdkZJwzZyLbz4E130_assertion
a
np:Assertion
.
dgn-np:NP797602.RAgg_H4TXau2Wi8ZDwS6biyb71g96fusdkZJwzZyLbz4E130_provenance
a
np:Provenance
.
dgn-np:NP797602.RAgg_H4TXau2Wi8ZDwS6biyb71g96fusdkZJwzZyLbz4E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP797602.RAgg_H4TXau2Wi8ZDwS6biyb71g96fusdkZJwzZyLbz4E130_assertion
{
miriam-gene:57379
a
ncit:C16612
.
lld:C1306589
a
ncit:C7057
.
dgn-gda:DGNa7582cc6c2fa17c30f895967c2389231
sio:SIO_000628
miriam-gene:57379
,
lld:C1306589
;
a
sio:SIO_001121
.
}
dgn-np:NP797602.RAgg_H4TXau2Wi8ZDwS6biyb71g96fusdkZJwzZyLbz4E130_provenance
{
dgn-np:NP797602.RAgg_H4TXau2Wi8ZDwS6biyb71g96fusdkZJwzZyLbz4E130_assertion
dcterms:description
"[Three main types of CDA have been distinguished: CDA I and CDA III, whose loci have been already mapped, and CDA II (MIM 224100), the most frequent among CDAs, which is transmitted as an autosomal recessive trait and is known also as `HEMPAS` (hereditary erythroblast multinuclearity with positive acidified serum).]. 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:9345103
;
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:NP797602.RAgg_H4TXau2Wi8ZDwS6biyb71g96fusdkZJwzZyLbz4E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:09+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" .
}