@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP677298.RAeobgKhYAe_TUWecxM_4y9DM90xIIYR3lrsvLBBpAPFc
> .
@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:NP677298.RAeobgKhYAe_TUWecxM_4y9DM90xIIYR3lrsvLBBpAPFc130_head
{
this:
np:hasAssertion
dgn-np:NP677298.RAeobgKhYAe_TUWecxM_4y9DM90xIIYR3lrsvLBBpAPFc130_assertion
;
np:hasProvenance
dgn-np:NP677298.RAeobgKhYAe_TUWecxM_4y9DM90xIIYR3lrsvLBBpAPFc130_provenance
;
np:hasPublicationInfo
dgn-np:NP677298.RAeobgKhYAe_TUWecxM_4y9DM90xIIYR3lrsvLBBpAPFc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP677298.RAeobgKhYAe_TUWecxM_4y9DM90xIIYR3lrsvLBBpAPFc130_assertion
a
np:Assertion
.
dgn-np:NP677298.RAeobgKhYAe_TUWecxM_4y9DM90xIIYR3lrsvLBBpAPFc130_provenance
a
np:Provenance
.
dgn-np:NP677298.RAeobgKhYAe_TUWecxM_4y9DM90xIIYR3lrsvLBBpAPFc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP677298.RAeobgKhYAe_TUWecxM_4y9DM90xIIYR3lrsvLBBpAPFc130_assertion
{
miriam-gene:5730
a
ncit:C16612
.
lld:C0546969
a
ncit:C7057
.
dgn-gda:DGNee1b69aa5a4b8e7ddc9451d14a5167dd
sio:SIO_000628
miriam-gene:5730
,
lld:C0546969
;
a
sio:SIO_001121
.
}
dgn-np:NP677298.RAeobgKhYAe_TUWecxM_4y9DM90xIIYR3lrsvLBBpAPFc130_provenance
{
dgn-np:NP677298.RAeobgKhYAe_TUWecxM_4y9DM90xIIYR3lrsvLBBpAPFc130_assertion
dcterms: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:NP677298.RAeobgKhYAe_TUWecxM_4y9DM90xIIYR3lrsvLBBpAPFc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:48+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" .
}