@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP625779.RA3fEPvMcDCAtoIt3hA9tWJ4DdgLVXS6_njDP93YB-XW8
> .
@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:NP625779.RA3fEPvMcDCAtoIt3hA9tWJ4DdgLVXS6_njDP93YB-XW8130_head
{
this:
np:hasAssertion
dgn-np:NP625779.RA3fEPvMcDCAtoIt3hA9tWJ4DdgLVXS6_njDP93YB-XW8130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP625779.RA3fEPvMcDCAtoIt3hA9tWJ4DdgLVXS6_njDP93YB-XW8130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP625779.RA3fEPvMcDCAtoIt3hA9tWJ4DdgLVXS6_njDP93YB-XW8130_assertion
a
np:Assertion
.
dgn-np:NP625779.RA3fEPvMcDCAtoIt3hA9tWJ4DdgLVXS6_njDP93YB-XW8130_provenance
a
np:Provenance
.
dgn-np:NP625779.RA3fEPvMcDCAtoIt3hA9tWJ4DdgLVXS6_njDP93YB-XW8130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:80184
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGNd82cdb85e4fde526e9d362e2d85d7f1c
sio:SIO_000628
miriam-gene:80184
,
lld:C0000768
;
a
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.
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dgn-np:NP625779.RA3fEPvMcDCAtoIt3hA9tWJ4DdgLVXS6_njDP93YB-XW8130_provenance
{
dgn-np:NP625779.RA3fEPvMcDCAtoIt3hA9tWJ4DdgLVXS6_njDP93YB-XW8130_assertion
dcterms:description
"[Our findings add to the increasing body of evidence that ciliopathies can cause a broad spectrum of disease phenotypes, and pleiotropic effects of CEP290 mutations range from single organ involvement with isolated Leber congenital amaurosis to Joubert syndrome and lethal early embryonic multisystemic malformations in Meckel-Gruber syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:17705300
;
prov:wasDerivedFrom
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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 .
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dgn-np:NP625779.RA3fEPvMcDCAtoIt3hA9tWJ4DdgLVXS6_njDP93YB-XW8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:29+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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