@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP88887.RA_OcVmOGWP4sHTAbGuILt64lxT-BlRZWD-9lTbWZk0m0
> .
@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/v3.0.0/void/
> .
dgn-np:NP88887.RA_OcVmOGWP4sHTAbGuILt64lxT-BlRZWD-9lTbWZk0m0130_head
{
this:
np:hasAssertion
dgn-np:NP88887.RA_OcVmOGWP4sHTAbGuILt64lxT-BlRZWD-9lTbWZk0m0130_assertion
;
np:hasProvenance
dgn-np:NP88887.RA_OcVmOGWP4sHTAbGuILt64lxT-BlRZWD-9lTbWZk0m0130_provenance
;
np:hasPublicationInfo
dgn-np:NP88887.RA_OcVmOGWP4sHTAbGuILt64lxT-BlRZWD-9lTbWZk0m0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP88887.RA_OcVmOGWP4sHTAbGuILt64lxT-BlRZWD-9lTbWZk0m0130_assertion
a
np:Assertion
.
dgn-np:NP88887.RA_OcVmOGWP4sHTAbGuILt64lxT-BlRZWD-9lTbWZk0m0130_provenance
a
np:Provenance
.
dgn-np:NP88887.RA_OcVmOGWP4sHTAbGuILt64lxT-BlRZWD-9lTbWZk0m0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP88887.RA_OcVmOGWP4sHTAbGuILt64lxT-BlRZWD-9lTbWZk0m0130_assertion
{
miriam-gene:5265
a
ncit:C16612
.
lld:C0010200
a
ncit:C7057
.
dgn-gda:DGNda3601e89d0358dca56f2e55f830eda0
sio:SIO_000628
miriam-gene:5265
,
lld:C0010200
;
a
sio:SIO_001122
.
}
dgn-np:NP88887.RA_OcVmOGWP4sHTAbGuILt64lxT-BlRZWD-9lTbWZk0m0130_provenance
{
dgn-np:NP88887.RA_OcVmOGWP4sHTAbGuILt64lxT-BlRZWD-9lTbWZk0m0130_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:NP88887.RA_OcVmOGWP4sHTAbGuILt64lxT-BlRZWD-9lTbWZk0m0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:29+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}