@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP138185.RAeX5ER75dSyyDsd69IyEpr4wB__cvVKjKoq2bBpF0-Hw
> .
@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:NP138185.RAeX5ER75dSyyDsd69IyEpr4wB__cvVKjKoq2bBpF0-Hw130_head
{
this:
np:hasAssertion
dgn-np:NP138185.RAeX5ER75dSyyDsd69IyEpr4wB__cvVKjKoq2bBpF0-Hw130_assertion
;
np:hasProvenance
dgn-np:NP138185.RAeX5ER75dSyyDsd69IyEpr4wB__cvVKjKoq2bBpF0-Hw130_provenance
;
np:hasPublicationInfo
dgn-np:NP138185.RAeX5ER75dSyyDsd69IyEpr4wB__cvVKjKoq2bBpF0-Hw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP138185.RAeX5ER75dSyyDsd69IyEpr4wB__cvVKjKoq2bBpF0-Hw130_assertion
a
np:Assertion
.
dgn-np:NP138185.RAeX5ER75dSyyDsd69IyEpr4wB__cvVKjKoq2bBpF0-Hw130_provenance
a
np:Provenance
.
dgn-np:NP138185.RAeX5ER75dSyyDsd69IyEpr4wB__cvVKjKoq2bBpF0-Hw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP138185.RAeX5ER75dSyyDsd69IyEpr4wB__cvVKjKoq2bBpF0-Hw130_assertion
{
miriam-gene:7439
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGNa267cbbc5fec8aaa05a035a4686b74c0
sio:SIO_000628
miriam-gene:7439
,
lld:C0242383
;
a
sio:SIO_001122
.
}
dgn-np:NP138185.RAeX5ER75dSyyDsd69IyEpr4wB__cvVKjKoq2bBpF0-Hw130_provenance
{
dgn-np:NP138185.RAeX5ER75dSyyDsd69IyEpr4wB__cvVKjKoq2bBpF0-Hw130_assertion
dcterms:description
"[Understanding the structure of the anion conduction pathway of bestrophins provides insights into how mutations produce channel dysfunction and may provide important information for development of therapeutic strategies for treating macular degeneration.]. 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:16707793
;
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:NP138185.RAeX5ER75dSyyDsd69IyEpr4wB__cvVKjKoq2bBpF0-Hw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:12+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" .
}