@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP64847.RARfNFXafMVnQsIyq-IjKzlh1kzElfmOg_4oisumbDD-g
> .
@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:NP64847.RARfNFXafMVnQsIyq-IjKzlh1kzElfmOg_4oisumbDD-g130_head
{
this:
np:hasAssertion
dgn-np:NP64847.RARfNFXafMVnQsIyq-IjKzlh1kzElfmOg_4oisumbDD-g130_assertion
;
np:hasProvenance
dgn-np:NP64847.RARfNFXafMVnQsIyq-IjKzlh1kzElfmOg_4oisumbDD-g130_provenance
;
np:hasPublicationInfo
dgn-np:NP64847.RARfNFXafMVnQsIyq-IjKzlh1kzElfmOg_4oisumbDD-g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP64847.RARfNFXafMVnQsIyq-IjKzlh1kzElfmOg_4oisumbDD-g130_assertion
a
np:Assertion
.
dgn-np:NP64847.RARfNFXafMVnQsIyq-IjKzlh1kzElfmOg_4oisumbDD-g130_provenance
a
np:Provenance
.
dgn-np:NP64847.RARfNFXafMVnQsIyq-IjKzlh1kzElfmOg_4oisumbDD-g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP64847.RARfNFXafMVnQsIyq-IjKzlh1kzElfmOg_4oisumbDD-g130_assertion
{
miriam-gene:5265
a
ncit:C16612
.
lld:C0221757
a
ncit:C7057
.
dgn-gda:DGN1dd711c49b36e648f67f6c3475944fe4
sio:SIO_000628
miriam-gene:5265
,
lld:C0221757
;
a
sio:SIO_001122
.
}
dgn-np:NP64847.RARfNFXafMVnQsIyq-IjKzlh1kzElfmOg_4oisumbDD-g130_provenance
{
dgn-np:NP64847.RARfNFXafMVnQsIyq-IjKzlh1kzElfmOg_4oisumbDD-g130_assertion
dcterms:description
"[Therefore, the optimal strategy for diagnostics of AAT deficiency should encompass detection of the most common AAT variants by IEF and screening for the less common variants by DGGE in combination with sequencing.]. 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:18433707
;
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:NP64847.RARfNFXafMVnQsIyq-IjKzlh1kzElfmOg_4oisumbDD-g130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:15+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" .
}