@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI
> .
@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/v3.0.0/void/
> .
dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_head
{
this:
np:hasAssertion
dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_assertion
;
np:hasProvenance
dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_provenance
;
np:hasPublicationInfo
dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_assertion
a
np:Assertion
.
dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_provenance
a
np:Provenance
.
dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_assertion
{
miriam-gene:80184
a
ncit:C16612
.
lld:C0431399
a
ncit:C7057
.
dgn-gda:DGN2ba0769591494d288ebd63f762719ba3
sio:SIO_000628
miriam-gene:80184
,
lld:C0431399
;
a
sio:SIO_001121
.
}
dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_provenance
{
dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_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 ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:17705300
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:19+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}