@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q
> .
@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:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_head
{
this:
np:hasAssertion
dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_assertion
;
np:hasProvenance
dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_assertion
a
np:Assertion
.
dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_provenance
a
np:Provenance
.
dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_assertion
{
miriam-gene:100128922
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGNaf553e69965800e202972e24e0815930
sio:SIO_000628
miriam-gene:100128922
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_provenance
{
dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_assertion
dcterms:description
"[It is important to consider connexin deafness in any child with recessive nonsyndromic hearing loss as well as simplex cases with no history of other affected family members even when the newborn hearing screening results were within the normal range.]. 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:17086082
;
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:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}