@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP420074.RAFhHd2NXWrU_Z4KWP9flOKABz5VM0DJgDm3HGjTIx4HE
> .
@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:NP420074.RAFhHd2NXWrU_Z4KWP9flOKABz5VM0DJgDm3HGjTIx4HE130_head
{
this:
np:hasAssertion
dgn-np:NP420074.RAFhHd2NXWrU_Z4KWP9flOKABz5VM0DJgDm3HGjTIx4HE130_assertion
;
np:hasProvenance
dgn-np:NP420074.RAFhHd2NXWrU_Z4KWP9flOKABz5VM0DJgDm3HGjTIx4HE130_provenance
;
np:hasPublicationInfo
dgn-np:NP420074.RAFhHd2NXWrU_Z4KWP9flOKABz5VM0DJgDm3HGjTIx4HE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP420074.RAFhHd2NXWrU_Z4KWP9flOKABz5VM0DJgDm3HGjTIx4HE130_assertion
a
np:Assertion
.
dgn-np:NP420074.RAFhHd2NXWrU_Z4KWP9flOKABz5VM0DJgDm3HGjTIx4HE130_provenance
a
np:Provenance
.
dgn-np:NP420074.RAFhHd2NXWrU_Z4KWP9flOKABz5VM0DJgDm3HGjTIx4HE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP420074.RAFhHd2NXWrU_Z4KWP9flOKABz5VM0DJgDm3HGjTIx4HE130_assertion
{
miriam-gene:100128922
a
ncit:C16612
.
lld:C0158945
a
ncit:C7057
.
dgn-gda:DGNc4ba91396897fbd0472ac5fe80d1e02b
sio:SIO_000628
miriam-gene:100128922
,
lld:C0158945
;
a
sio:SIO_001121
.
}
dgn-np:NP420074.RAFhHd2NXWrU_Z4KWP9flOKABz5VM0DJgDm3HGjTIx4HE130_provenance
{
dgn-np:NP420074.RAFhHd2NXWrU_Z4KWP9flOKABz5VM0DJgDm3HGjTIx4HE130_assertion
dcterms:description
"[Congenital CMV infections and connexin mutations are the two major causes of deafness at birth, while causes for enlarged vestibular aqueduct along with congenital CMV infection are the major causes of pre-lingual hearing loss that is not expressed at birth.]. 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:16384744
;
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:NP420074.RAFhHd2NXWrU_Z4KWP9flOKABz5VM0DJgDm3HGjTIx4HE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:09+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" .
}