@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP369949.RA66uvrsTL2tyLUc4hRXFoC0dCJWBELGWOiksgFy9pKb8
> .
@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:NP369949.RA66uvrsTL2tyLUc4hRXFoC0dCJWBELGWOiksgFy9pKb8130_head
{
this:
np:hasAssertion
dgn-np:NP369949.RA66uvrsTL2tyLUc4hRXFoC0dCJWBELGWOiksgFy9pKb8130_assertion
;
np:hasProvenance
dgn-np:NP369949.RA66uvrsTL2tyLUc4hRXFoC0dCJWBELGWOiksgFy9pKb8130_provenance
;
np:hasPublicationInfo
dgn-np:NP369949.RA66uvrsTL2tyLUc4hRXFoC0dCJWBELGWOiksgFy9pKb8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP369949.RA66uvrsTL2tyLUc4hRXFoC0dCJWBELGWOiksgFy9pKb8130_assertion
a
np:Assertion
.
dgn-np:NP369949.RA66uvrsTL2tyLUc4hRXFoC0dCJWBELGWOiksgFy9pKb8130_provenance
a
np:Provenance
.
dgn-np:NP369949.RA66uvrsTL2tyLUc4hRXFoC0dCJWBELGWOiksgFy9pKb8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP369949.RA66uvrsTL2tyLUc4hRXFoC0dCJWBELGWOiksgFy9pKb8130_assertion
{
miriam-gene:5265
a
ncit:C16612
.
lld:C0024115
a
ncit:C7057
.
dgn-gda:DGNc69a49f04ae6bc6fa6f61db1d4997ab7
sio:SIO_000628
miriam-gene:5265
,
lld:C0024115
;
a
sio:SIO_001121
.
}
dgn-np:NP369949.RA66uvrsTL2tyLUc4hRXFoC0dCJWBELGWOiksgFy9pKb8130_provenance
{
dgn-np:NP369949.RA66uvrsTL2tyLUc4hRXFoC0dCJWBELGWOiksgFy9pKb8130_assertion
dcterms:description
"[In this review, we will define further the diagnosis of alpha1AT deficiency and its clinical manifestations and describe the therapeutic strategies that are currently being developed to treat the hepatic and pulmonary disease associated with this condition.]. 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:11202478
;
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:NP369949.RA66uvrsTL2tyLUc4hRXFoC0dCJWBELGWOiksgFy9pKb8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:36+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" .
}