@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP697158.RAt4aglVEI4OgpvdYVfDDhvLRKCpEKp9z3CT2v_qxkk2c
> .
@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:NP697158.RAt4aglVEI4OgpvdYVfDDhvLRKCpEKp9z3CT2v_qxkk2c130_head
{
this:
np:hasAssertion
dgn-np:NP697158.RAt4aglVEI4OgpvdYVfDDhvLRKCpEKp9z3CT2v_qxkk2c130_assertion
;
np:hasProvenance
dgn-np:NP697158.RAt4aglVEI4OgpvdYVfDDhvLRKCpEKp9z3CT2v_qxkk2c130_provenance
;
np:hasPublicationInfo
dgn-np:NP697158.RAt4aglVEI4OgpvdYVfDDhvLRKCpEKp9z3CT2v_qxkk2c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP697158.RAt4aglVEI4OgpvdYVfDDhvLRKCpEKp9z3CT2v_qxkk2c130_assertion
a
np:Assertion
.
dgn-np:NP697158.RAt4aglVEI4OgpvdYVfDDhvLRKCpEKp9z3CT2v_qxkk2c130_provenance
a
np:Provenance
.
dgn-np:NP697158.RAt4aglVEI4OgpvdYVfDDhvLRKCpEKp9z3CT2v_qxkk2c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP697158.RAt4aglVEI4OgpvdYVfDDhvLRKCpEKp9z3CT2v_qxkk2c130_assertion
{
miriam-gene:10423
a
ncit:C16612
.
lld:C0221757
a
ncit:C7057
.
dgn-gda:DGN8b242e99b227467b56c6273adcb94562
sio:SIO_000628
miriam-gene:10423
,
lld:C0221757
;
a
sio:SIO_001121
.
}
dgn-np:NP697158.RAt4aglVEI4OgpvdYVfDDhvLRKCpEKp9z3CT2v_qxkk2c130_provenance
{
dgn-np:NP697158.RAt4aglVEI4OgpvdYVfDDhvLRKCpEKp9z3CT2v_qxkk2c130_assertion
dcterms:description
"[Our studies demonstrated striking differences in the prevalence of both the PIS and PIZ alleles among these 25 countries in the Caribbean and North, Central and South America and significant numbers of individuals at risk for adverse health effects associated with AAT Deficiency in a given country.]. 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:19999955
;
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:NP697158.RAt4aglVEI4OgpvdYVfDDhvLRKCpEKp9z3CT2v_qxkk2c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:04+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" .
}