@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA
> .
@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:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_head
{
this:
np:hasAssertion
dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_assertion
;
np:hasProvenance
dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_provenance
;
np:hasPublicationInfo
dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_assertion
a
np:Assertion
.
dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_provenance
a
np:Provenance
.
dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_assertion
{
miriam-gene:51364
a
ncit:C16612
.
lld:C0022679
a
ncit:C7057
.
dgn-gda:DGNefb6e69d9e1b41da769c0b46abc9da59
sio:SIO_000628
miriam-gene:51364
,
lld:C0022679
;
a
sio:SIO_001121
.
}
dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_provenance
{
dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_assertion
dcterms:description
"[Animal models support the association between ZMYND10 and human PCD, given that zmynd10 knockdown in zebrafish caused ciliary paralysis leading to cystic kidneys and otolith defects and that knockdown in Xenopus interfered with ciliogenesis.]. 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:23891469
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}