@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP181365.RAdUxILIjiQvLm558_u-Rg76XamyuwnOsj3e6dK-Ko2hQ
> .
@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:NP181365.RAdUxILIjiQvLm558_u-Rg76XamyuwnOsj3e6dK-Ko2hQ130_head
{
this:
np:hasAssertion
dgn-np:NP181365.RAdUxILIjiQvLm558_u-Rg76XamyuwnOsj3e6dK-Ko2hQ130_assertion
;
np:hasProvenance
dgn-np:NP181365.RAdUxILIjiQvLm558_u-Rg76XamyuwnOsj3e6dK-Ko2hQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP181365.RAdUxILIjiQvLm558_u-Rg76XamyuwnOsj3e6dK-Ko2hQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP181365.RAdUxILIjiQvLm558_u-Rg76XamyuwnOsj3e6dK-Ko2hQ130_assertion
a
np:Assertion
.
dgn-np:NP181365.RAdUxILIjiQvLm558_u-Rg76XamyuwnOsj3e6dK-Ko2hQ130_provenance
a
np:Provenance
.
dgn-np:NP181365.RAdUxILIjiQvLm558_u-Rg76XamyuwnOsj3e6dK-Ko2hQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP181365.RAdUxILIjiQvLm558_u-Rg76XamyuwnOsj3e6dK-Ko2hQ130_assertion
{
miriam-gene:5265
a
ncit:C16612
.
lld:C0024115
a
ncit:C7057
.
dgn-gda:DGN01dae80b4a09da723d2ae1ecbb4ee3ed
sio:SIO_000628
miriam-gene:5265
,
lld:C0024115
;
a
sio:SIO_001121
.
}
dgn-np:NP181365.RAdUxILIjiQvLm558_u-Rg76XamyuwnOsj3e6dK-Ko2hQ130_provenance
{
dgn-np:NP181365.RAdUxILIjiQvLm558_u-Rg76XamyuwnOsj3e6dK-Ko2hQ130_assertion
dcterms:description
"[The c.-1973T >C polymorphism located in the SERPINA1 promoter region is found more frequent in A1AT deficiency patients with liver disease compared to patients with pulmonary disease, but data are lacking regarding contribution to the development of liver diseases caused by other aetiologies.]. 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:20170533
;
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:NP181365.RAdUxILIjiQvLm558_u-Rg76XamyuwnOsj3e6dK-Ko2hQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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" .
}