@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP184671.RAGir6PF-YPwmy-K5_QYqxT8A81pdMKKK8Tr30On9y90o
> .
@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:NP184671.RAGir6PF-YPwmy-K5_QYqxT8A81pdMKKK8Tr30On9y90o130_head
{
this:
np:hasAssertion
dgn-np:NP184671.RAGir6PF-YPwmy-K5_QYqxT8A81pdMKKK8Tr30On9y90o130_assertion
;
np:hasProvenance
dgn-np:NP184671.RAGir6PF-YPwmy-K5_QYqxT8A81pdMKKK8Tr30On9y90o130_provenance
;
np:hasPublicationInfo
dgn-np:NP184671.RAGir6PF-YPwmy-K5_QYqxT8A81pdMKKK8Tr30On9y90o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP184671.RAGir6PF-YPwmy-K5_QYqxT8A81pdMKKK8Tr30On9y90o130_assertion
a
np:Assertion
.
dgn-np:NP184671.RAGir6PF-YPwmy-K5_QYqxT8A81pdMKKK8Tr30On9y90o130_provenance
a
np:Provenance
.
dgn-np:NP184671.RAGir6PF-YPwmy-K5_QYqxT8A81pdMKKK8Tr30On9y90o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP184671.RAGir6PF-YPwmy-K5_QYqxT8A81pdMKKK8Tr30On9y90o130_assertion
{
miriam-gene:2707
a
ncit:C16612
.
lld:C0022596
a
ncit:C7057
.
dgn-gda:DGN2e4ae9ad1c13facb9e0cee104985503c
sio:SIO_000628
miriam-gene:2707
,
lld:C0022596
;
a
sio:SIO_001121
.
}
dgn-np:NP184671.RAGir6PF-YPwmy-K5_QYqxT8A81pdMKKK8Tr30On9y90o130_provenance
{
dgn-np:NP184671.RAGir6PF-YPwmy-K5_QYqxT8A81pdMKKK8Tr30On9y90o130_assertion
dcterms:description
"[The importance of gap junctional intercellular communication for normal development and differentiation of human epidermis as well as the hearing function of the inner ear is illustrated by the examples of erythrokeratodermia variabilis and palmoplantar keratoderma associated with hearing loss.]. 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:10772382
;
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:NP184671.RAGir6PF-YPwmy-K5_QYqxT8A81pdMKKK8Tr30On9y90o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:40+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" .
}