@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM
> .
@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 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:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_head
{
this:
np:hasAssertion
dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_assertion
;
np:hasProvenance
dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_provenance
;
np:hasPublicationInfo
dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_assertion
a
np:Assertion
.
dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_provenance
a
np:Provenance
.
dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_assertion
{
miriam-gene:8909
a
ncit:C16612
.
lld:C0018852
a
ncit:C7057
.
dgn-gda:DGNe5e877d87fb4c6e10c67d50b2b4fd6fa
sio:SIO_000628
miriam-gene:8909
,
lld:C0018852
;
a
sio:SIO_001121
.
}
dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_provenance
{
dgn-np:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_assertion
dct:description
"[Alpha heavy chain diseases (HCD) are lymphoproliferative disorders characterized by the production of truncated alpha immunoglobulin heavy chain without associated light chains, alpha HCD MAL is featured by multiple structural alterations of the alpha 1 productive gene and on original t(9;14)(p11;q32) translocation involving the other rearranged alpha 1 allele.]. 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:2125275
;
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:NP364440.RADr0kyEU9vfhUQ0n1brvQ5S5wexUpdz5u75ktZnCuIZM130_publicationInfo
{
this:
dct:created
"2014-10-02T12:35:33+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}