@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP886251.RAFKEMDo9etJx-mgiBYdY6G77jIy_F8fvlnXWJRDxGgvE
> .
@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:NP886251.RAFKEMDo9etJx-mgiBYdY6G77jIy_F8fvlnXWJRDxGgvE130_head
{
this:
np:hasAssertion
dgn-np:NP886251.RAFKEMDo9etJx-mgiBYdY6G77jIy_F8fvlnXWJRDxGgvE130_assertion
;
np:hasProvenance
dgn-np:NP886251.RAFKEMDo9etJx-mgiBYdY6G77jIy_F8fvlnXWJRDxGgvE130_provenance
;
np:hasPublicationInfo
dgn-np:NP886251.RAFKEMDo9etJx-mgiBYdY6G77jIy_F8fvlnXWJRDxGgvE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP886251.RAFKEMDo9etJx-mgiBYdY6G77jIy_F8fvlnXWJRDxGgvE130_assertion
a
np:Assertion
.
dgn-np:NP886251.RAFKEMDo9etJx-mgiBYdY6G77jIy_F8fvlnXWJRDxGgvE130_provenance
a
np:Provenance
.
dgn-np:NP886251.RAFKEMDo9etJx-mgiBYdY6G77jIy_F8fvlnXWJRDxGgvE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP886251.RAFKEMDo9etJx-mgiBYdY6G77jIy_F8fvlnXWJRDxGgvE130_assertion
{
miriam-gene:27130
a
ncit:C16612
.
lld:C0752166
a
ncit:C7057
.
dgn-gda:DGN180a0e088e573229f7381cbe8c580d50
sio:SIO_000628
miriam-gene:27130
,
lld:C0752166
;
a
sio:SIO_001121
.
}
dgn-np:NP886251.RAFKEMDo9etJx-mgiBYdY6G77jIy_F8fvlnXWJRDxGgvE130_provenance
{
dgn-np:NP886251.RAFKEMDo9etJx-mgiBYdY6G77jIy_F8fvlnXWJRDxGgvE130_assertion
dcterms:description
"[Cilia are comprised of distinct structural and functional subregions including the basal body, transition zone (TZ) and inversin (Inv) compartments, and defects in this organelle are associated with an expanding spectrum of inherited disorders including Bardet-Biedl syndrome (BBS), Meckel-Gruber Syndrome (MKS), Joubert Syndrome (JS) and Nephronophthisis (NPHP).]. 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:24339792
;
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:NP886251.RAFKEMDo9etJx-mgiBYdY6G77jIy_F8fvlnXWJRDxGgvE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:40+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" .
}