@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP553638.RAau-4LIKo-zHYXhS45WyB30i69tpHhFhQhxTyeqQegN4
> .
@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:NP553638.RAau-4LIKo-zHYXhS45WyB30i69tpHhFhQhxTyeqQegN4130_head
{
this:
np:hasAssertion
dgn-np:NP553638.RAau-4LIKo-zHYXhS45WyB30i69tpHhFhQhxTyeqQegN4130_assertion
;
np:hasProvenance
dgn-np:NP553638.RAau-4LIKo-zHYXhS45WyB30i69tpHhFhQhxTyeqQegN4130_provenance
;
np:hasPublicationInfo
dgn-np:NP553638.RAau-4LIKo-zHYXhS45WyB30i69tpHhFhQhxTyeqQegN4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP553638.RAau-4LIKo-zHYXhS45WyB30i69tpHhFhQhxTyeqQegN4130_assertion
a
np:Assertion
.
dgn-np:NP553638.RAau-4LIKo-zHYXhS45WyB30i69tpHhFhQhxTyeqQegN4130_provenance
a
np:Provenance
.
dgn-np:NP553638.RAau-4LIKo-zHYXhS45WyB30i69tpHhFhQhxTyeqQegN4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP553638.RAau-4LIKo-zHYXhS45WyB30i69tpHhFhQhxTyeqQegN4130_assertion
{
miriam-gene:2201
a
ncit:C16612
.
lld:C0220668
a
ncit:C7057
.
dgn-gda:DGNa88be6574addfcbe1623ee87d2e057df
sio:SIO_000628
miriam-gene:2201
,
lld:C0220668
;
a
sio:SIO_001121
.
}
dgn-np:NP553638.RAau-4LIKo-zHYXhS45WyB30i69tpHhFhQhxTyeqQegN4130_provenance
{
dgn-np:NP553638.RAau-4LIKo-zHYXhS45WyB30i69tpHhFhQhxTyeqQegN4130_assertion
dcterms:description
"[One patient with a small deletion involving SDCCAG8 and AKT3, and another patient with an intragenic deletion of AKT3 did not have any CCA, implying that the loss of these two genes is unlikely to be the cause of CCA.]. 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:21934713
;
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:NP553638.RAau-4LIKo-zHYXhS45WyB30i69tpHhFhQhxTyeqQegN4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:34+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" .
}