@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg
> .
@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:NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_head
{
this:
np:hasAssertion
dgn-np:NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_assertion
;
np:hasProvenance
dgn-np:NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_provenance
;
np:hasPublicationInfo
dgn-np:NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_assertion
a
np:Assertion
.
dgn-np:NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_provenance
a
np:Provenance
.
dgn-np:NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_assertion
{
miriam-gene:100
a
ncit:C16612
.
lld:C0392607
a
ncit:C7057
.
dgn-gda:DGN8b6fd7a4eb79b266d464a8be858861dd
sio:SIO_000628
miriam-gene:100
,
lld:C0392607
;
a
sio:SIO_001121
.
}
dgn-np:NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_provenance
{
dgn-np:NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_assertion
dcterms:description
"[ADA deficiency in at least two mutant cell lines is not caused by deficient levels of translatable mRNA, and unless there is some translational control of this mRNA, the characteristic cellular ADA deficiency is most likely secondary to synthesis and rapid degradation of a defective ADA protein.]. 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:6134754
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1304806.RASDpeG1lhdi-3nkaVMsfevzklzX-PfpR8myguilaaLhg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:37+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" .
}