@prefix bfo: <
http://purl.obolibrary.org/obo/
> .
@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP237110.RAHbNh9enLDpHtr4EiyCC-AbByD7TzKuLnWsSUOFIKIg0
> .
@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 wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP237110.RAHbNh9enLDpHtr4EiyCC-AbByD7TzKuLnWsSUOFIKIg0130_head
{
this:
np:hasAssertion
dgn-np:NP237110.RAHbNh9enLDpHtr4EiyCC-AbByD7TzKuLnWsSUOFIKIg0130_assertion
;
np:hasProvenance
dgn-np:NP237110.RAHbNh9enLDpHtr4EiyCC-AbByD7TzKuLnWsSUOFIKIg0130_provenance
;
np:hasPublicationInfo
dgn-np:NP237110.RAHbNh9enLDpHtr4EiyCC-AbByD7TzKuLnWsSUOFIKIg0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP237110.RAHbNh9enLDpHtr4EiyCC-AbByD7TzKuLnWsSUOFIKIg0130_assertion
a
np:Assertion
.
dgn-np:NP237110.RAHbNh9enLDpHtr4EiyCC-AbByD7TzKuLnWsSUOFIKIg0130_provenance
a
np:Provenance
.
dgn-np:NP237110.RAHbNh9enLDpHtr4EiyCC-AbByD7TzKuLnWsSUOFIKIg0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP237110.RAHbNh9enLDpHtr4EiyCC-AbByD7TzKuLnWsSUOFIKIg0130_assertion
{
miriam-gene:2248
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGN14bee43ffc399409b83f44ef2055eaff
sio:SIO_000628
miriam-gene:2248
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP237110.RAHbNh9enLDpHtr4EiyCC-AbByD7TzKuLnWsSUOFIKIg0130_provenance
{
dgn-np:NP237110.RAHbNh9enLDpHtr4EiyCC-AbByD7TzKuLnWsSUOFIKIg0130_assertion
dcterms:description
"[sequenced the FGF3 gene in 10 unrelated families in which probands had congenital deafness associated with various inner ear anomalies, including Michel aplasia, with or without tooth or external ear anomalies.]. 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:18435799
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
bfo:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
xsd:date
.
dgn-void:source_evidence_literature
a
bfo:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP237110.RAHbNh9enLDpHtr4EiyCC-AbByD7TzKuLnWsSUOFIKIg0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:33+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}