@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A
> .
@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:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_head
{
this:
np:hasAssertion
dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_assertion
;
np:hasProvenance
dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_provenance
;
np:hasPublicationInfo
dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_assertion
a
np:Assertion
.
dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_provenance
a
np:Provenance
.
dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0024299
a
ncit:C7057
.
dgn-gda:DGN82e701e0e31dcdf0463b02895d6f6469
sio:SIO_000628
miriam-gene:4397
,
lld:C0024299
;
a
sio:SIO_001121
.
}
dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_provenance
{
dgn-np:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_assertion
dcterms:description
"[The distribution of ALlambda deposits in these 3 cases indicates that widespread subcortical vascular amyloidosis with leukoencephalopathy is a novel clinicopathologic entity distinguished from other cerebral diseases with local amyloid light chain deposition, including amyloidoma, leptomeningeal vascular amyloidosis, solitary intracerebral plasmacytoma, primary intracerebral lymphoma with plasmacytic differentiation, and multiple sclerosis with demyelination-associated amyloid deposition.]. 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:19225408
;
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:NP414337.RAGQrIaemdSb3cPvp30H-o-Ji7VSy-l1vm3wufB5eRl9A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:06+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
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}