@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP139884.RAPSDsuP5CZF5ch2A9Ae3_GmGmSYvJ4w7fTKCYPSDiU1o
> .
@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/
> .
dgn-np:NP139884.RAPSDsuP5CZF5ch2A9Ae3_GmGmSYvJ4w7fTKCYPSDiU1o130_head
{
this:
np:hasAssertion
dgn-np:NP139884.RAPSDsuP5CZF5ch2A9Ae3_GmGmSYvJ4w7fTKCYPSDiU1o130_assertion
;
np:hasProvenance
dgn-np:NP139884.RAPSDsuP5CZF5ch2A9Ae3_GmGmSYvJ4w7fTKCYPSDiU1o130_provenance
;
np:hasPublicationInfo
dgn-np:NP139884.RAPSDsuP5CZF5ch2A9Ae3_GmGmSYvJ4w7fTKCYPSDiU1o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP139884.RAPSDsuP5CZF5ch2A9Ae3_GmGmSYvJ4w7fTKCYPSDiU1o130_assertion
a
np:Assertion
.
dgn-np:NP139884.RAPSDsuP5CZF5ch2A9Ae3_GmGmSYvJ4w7fTKCYPSDiU1o130_provenance
a
np:Provenance
.
dgn-np:NP139884.RAPSDsuP5CZF5ch2A9Ae3_GmGmSYvJ4w7fTKCYPSDiU1o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP139884.RAPSDsuP5CZF5ch2A9Ae3_GmGmSYvJ4w7fTKCYPSDiU1o130_assertion
{
miriam-gene:5265
a
ncit:C16612
.
lld:C0024117
a
ncit:C7057
.
dgn-gda:DGN181e2131011e13b5d44db05bf26ec887
sio:SIO_000628
miriam-gene:5265
,
lld:C0024117
;
a
sio:SIO_001122
.
}
dgn-np:NP139884.RAPSDsuP5CZF5ch2A9Ae3_GmGmSYvJ4w7fTKCYPSDiU1o130_provenance
{
dgn-np:NP139884.RAPSDsuP5CZF5ch2A9Ae3_GmGmSYvJ4w7fTKCYPSDiU1o130_assertion
dcterms:description
"[Thirty patients presented AAT levels lower than the mean values found in patients with the MM or MS genotype, and this fact could not be explained by an increased frequency of S and Z alleles.]. 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:19180336
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP139884.RAPSDsuP5CZF5ch2A9Ae3_GmGmSYvJ4w7fTKCYPSDiU1o130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:51+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}