@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP924413.RAOYQs9JvUctkFt0S3YyJG3S-Yutj-Yjt6akSXnZAMdpg
> .
@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:NP924413.RAOYQs9JvUctkFt0S3YyJG3S-Yutj-Yjt6akSXnZAMdpg130_head
{
this:
np:hasAssertion
dgn-np:NP924413.RAOYQs9JvUctkFt0S3YyJG3S-Yutj-Yjt6akSXnZAMdpg130_assertion
;
np:hasProvenance
dgn-np:NP924413.RAOYQs9JvUctkFt0S3YyJG3S-Yutj-Yjt6akSXnZAMdpg130_provenance
;
np:hasPublicationInfo
dgn-np:NP924413.RAOYQs9JvUctkFt0S3YyJG3S-Yutj-Yjt6akSXnZAMdpg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP924413.RAOYQs9JvUctkFt0S3YyJG3S-Yutj-Yjt6akSXnZAMdpg130_assertion
a
np:Assertion
.
dgn-np:NP924413.RAOYQs9JvUctkFt0S3YyJG3S-Yutj-Yjt6akSXnZAMdpg130_provenance
a
np:Provenance
.
dgn-np:NP924413.RAOYQs9JvUctkFt0S3YyJG3S-Yutj-Yjt6akSXnZAMdpg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP924413.RAOYQs9JvUctkFt0S3YyJG3S-Yutj-Yjt6akSXnZAMdpg130_assertion
{
miriam-gene:146
a
ncit:C16612
.
lld:C0002949
a
ncit:C7057
.
dgn-gda:DGN4c8559ae605d2c4b7b04bc9578cb029f
sio:SIO_000628
miriam-gene:146
,
lld:C0002949
;
a
sio:SIO_001121
.
}
dgn-np:NP924413.RAOYQs9JvUctkFt0S3YyJG3S-Yutj-Yjt6akSXnZAMdpg130_provenance
{
dgn-np:NP924413.RAOYQs9JvUctkFt0S3YyJG3S-Yutj-Yjt6akSXnZAMdpg130_assertion
dcterms:description
"[We prospectively submitted to AAT serum levels determination, phenotyping and, if doubtful, genotyping: (i) patients with the early onset of emphysema, emphysema in absence of recognized risk or pneumothorax (path P), antineutrophil cytoplasm antibodies (ANCA) positive vasculitis (path V), cervical artery dissection (path A), Periodic acid-Schiff (PAS) positive bodies in the liver cell or unexplained abnormal transaminase level (Path L) [index cases: IC] and (ii) subjects with low-serum alpha1-globulin (path e) and close relatives of patients with AAT deficiency (path r) [non index cases: NIC].]. 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:16043335
;
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:NP924413.RAOYQs9JvUctkFt0S3YyJG3S-Yutj-Yjt6akSXnZAMdpg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:27+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" .
}