@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP960660.RACDx1kNZUzeAN0WITr2owwhnTsUhE_GCW2DjMWDmKGsM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP960660.RACDx1kNZUzeAN0WITr2owwhnTsUhE_GCW2DjMWDmKGsM130_assertion
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np:hasPublicationInfo
dgn-np:NP960660.RACDx1kNZUzeAN0WITr2owwhnTsUhE_GCW2DjMWDmKGsM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP960660.RACDx1kNZUzeAN0WITr2owwhnTsUhE_GCW2DjMWDmKGsM130_assertion
a
np:Assertion
.
dgn-np:NP960660.RACDx1kNZUzeAN0WITr2owwhnTsUhE_GCW2DjMWDmKGsM130_provenance
a
np:Provenance
.
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a
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{
miriam-gene:5265
a
ncit:C16612
.
lld:C0221757
a
ncit:C7057
.
dgn-gda:DGNc2ea9e88ab66e7c0db9c1ef814105e21
sio:SIO_000628
miriam-gene:5265
,
lld:C0221757
;
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.
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{
dgn-np:NP960660.RACDx1kNZUzeAN0WITr2owwhnTsUhE_GCW2DjMWDmKGsM130_assertion
dcterms:description
"[This report illustrates the diagnostic value of incorporating exon sequencing of the AAT gene into the algorithm for evaluating AATD, particularly when the AAT serum level is significantly lower than expected from IEF PI-typing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:22330941
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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 .
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dgn-np:NP960660.RACDx1kNZUzeAN0WITr2owwhnTsUhE_GCW2DjMWDmKGsM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:00+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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<
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
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<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v4.0.0.0" .
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"v4.0.0" .
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