@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw
> .
@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:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_head
{
this:
np:hasAssertion
dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_assertion
;
np:hasProvenance
dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_provenance
;
np:hasPublicationInfo
dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_assertion
a
np:Assertion
.
dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_provenance
a
np:Provenance
.
dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_assertion
{
miriam-gene:27130
a
ncit:C16612
.
lld:C0020258
a
ncit:C7057
.
dgn-gda:DGN176ea7d428d92fff20b59f580254471d
sio:SIO_000628
miriam-gene:27130
,
lld:C0020258
;
a
sio:SIO_001121
.
}
dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_provenance
{
dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_assertion
dcterms:description
"[Positional cloning and candidate gene approaches led to the identification of eight causative genes (NPHP1, 3, 4, 5, 6, 7, 8, and 9) responsible for the juvenile NPH and one gene NPHP2 for the infantile form.]. 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:18607645
;
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:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:35+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" .
}