@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP272079.RAc9ua355PWqvI3igzYBd1MEdDfzK4GhIiNtijhLo6APo
> .
@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:NP272079.RAc9ua355PWqvI3igzYBd1MEdDfzK4GhIiNtijhLo6APo130_head
{
this:
np:hasAssertion
dgn-np:NP272079.RAc9ua355PWqvI3igzYBd1MEdDfzK4GhIiNtijhLo6APo130_assertion
;
np:hasProvenance
dgn-np:NP272079.RAc9ua355PWqvI3igzYBd1MEdDfzK4GhIiNtijhLo6APo130_provenance
;
np:hasPublicationInfo
dgn-np:NP272079.RAc9ua355PWqvI3igzYBd1MEdDfzK4GhIiNtijhLo6APo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP272079.RAc9ua355PWqvI3igzYBd1MEdDfzK4GhIiNtijhLo6APo130_assertion
a
np:Assertion
.
dgn-np:NP272079.RAc9ua355PWqvI3igzYBd1MEdDfzK4GhIiNtijhLo6APo130_provenance
a
np:Provenance
.
dgn-np:NP272079.RAc9ua355PWqvI3igzYBd1MEdDfzK4GhIiNtijhLo6APo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP272079.RAc9ua355PWqvI3igzYBd1MEdDfzK4GhIiNtijhLo6APo130_assertion
{
miriam-gene:5053
a
ncit:C16612
.
lld:C0008533
a
ncit:C7057
.
dgn-gda:DGN6fc19682e36fb90109617c239d20729e
sio:SIO_000628
miriam-gene:5053
,
lld:C0008533
;
a
sio:SIO_001121
.
}
dgn-np:NP272079.RAc9ua355PWqvI3igzYBd1MEdDfzK4GhIiNtijhLo6APo130_provenance
{
dgn-np:NP272079.RAc9ua355PWqvI3igzYBd1MEdDfzK4GhIiNtijhLo6APo130_assertion
dcterms:description
"[The two diseases being used as models for hepatic gene therapy are classical phenylketonuria (PKU) and haemophilia B. Vectors derived from adenoviruses can be used to completely correct these diseases in animal models.]. 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:8884565
;
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:NP272079.RAc9ua355PWqvI3igzYBd1MEdDfzK4GhIiNtijhLo6APo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:33+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" .
}