@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP174823.RAAJUtY9vRASFIOdpdEe9faFH7tsNV5TlCkfP3vP5pRLQ
> .
@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 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:NP174823.RAAJUtY9vRASFIOdpdEe9faFH7tsNV5TlCkfP3vP5pRLQ130_head
{
this:
np:hasAssertion
dgn-np:NP174823.RAAJUtY9vRASFIOdpdEe9faFH7tsNV5TlCkfP3vP5pRLQ130_assertion
;
np:hasProvenance
dgn-np:NP174823.RAAJUtY9vRASFIOdpdEe9faFH7tsNV5TlCkfP3vP5pRLQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP174823.RAAJUtY9vRASFIOdpdEe9faFH7tsNV5TlCkfP3vP5pRLQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP174823.RAAJUtY9vRASFIOdpdEe9faFH7tsNV5TlCkfP3vP5pRLQ130_assertion
a
np:Assertion
.
dgn-np:NP174823.RAAJUtY9vRASFIOdpdEe9faFH7tsNV5TlCkfP3vP5pRLQ130_provenance
a
np:Provenance
.
dgn-np:NP174823.RAAJUtY9vRASFIOdpdEe9faFH7tsNV5TlCkfP3vP5pRLQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP174823.RAAJUtY9vRASFIOdpdEe9faFH7tsNV5TlCkfP3vP5pRLQ130_assertion
{
miriam-gene:2138
a
ncit:C16612
.
lld:C0546969
a
ncit:C7057
.
dgn-gda:DGNd34c39cd7911d597625f8f678c79ab51
sio:SIO_000628
miriam-gene:2138
,
lld:C0546969
;
a
sio:SIO_001121
.
}
dgn-np:NP174823.RAAJUtY9vRASFIOdpdEe9faFH7tsNV5TlCkfP3vP5pRLQ130_provenance
{
dgn-np:NP174823.RAAJUtY9vRASFIOdpdEe9faFH7tsNV5TlCkfP3vP5pRLQ130_assertion
dct:description
"[PDS mutations were found only in patients with enlarged vestibular aqueducts and EYA1 mutations were detected only in patients with ear pits and cervical fistulae, indicating that these two genes are associated with particular forms of middle and inner ear malformation.]. 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:11558900
;
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:NP174823.RAAJUtY9vRASFIOdpdEe9faFH7tsNV5TlCkfP3vP5pRLQ130_publicationInfo
{
this:
dct:created
"2014-10-02T12:33:34+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}