@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA
> .
@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:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_head
{
this:
np:hasAssertion
dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_assertion
;
np:hasProvenance
dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_provenance
;
np:hasPublicationInfo
dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_assertion
a
np:Assertion
.
dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_provenance
a
np:Provenance
.
dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_assertion
{
miriam-gene:9590
a
ncit:C16612
.
lld:C0035335
a
ncit:C7057
.
dgn-gda:DGN4731bef66453d86075f12eca38f93072
sio:SIO_000628
miriam-gene:9590
,
lld:C0035335
;
a
sio:SIO_001121
.
}
dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_provenance
{
dgn-np:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_assertion
dcterms:description
"[AKAP12 may induce BRB formation through antiangiogenesis and barriergenesis in developing human eye and defects in this mechanism can lead to loss of tight junction proteins and contribute to development of retinal pathologies such as retinoblastoma.]. 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:17442832
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP110179.RAZnUe34WeEjqHohl2myomRjOus_jt48QFSPw8HaMN2bA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:56+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" .
}