@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP188872.RAx22kZ6kPqEKut93iUi_QA-lazqbP09HXQKPC9TZTq1s
> .
@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:NP188872.RAx22kZ6kPqEKut93iUi_QA-lazqbP09HXQKPC9TZTq1s130_head
{
this:
np:hasAssertion
dgn-np:NP188872.RAx22kZ6kPqEKut93iUi_QA-lazqbP09HXQKPC9TZTq1s130_assertion
;
np:hasProvenance
dgn-np:NP188872.RAx22kZ6kPqEKut93iUi_QA-lazqbP09HXQKPC9TZTq1s130_provenance
;
np:hasPublicationInfo
dgn-np:NP188872.RAx22kZ6kPqEKut93iUi_QA-lazqbP09HXQKPC9TZTq1s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP188872.RAx22kZ6kPqEKut93iUi_QA-lazqbP09HXQKPC9TZTq1s130_assertion
a
np:Assertion
.
dgn-np:NP188872.RAx22kZ6kPqEKut93iUi_QA-lazqbP09HXQKPC9TZTq1s130_provenance
a
np:Provenance
.
dgn-np:NP188872.RAx22kZ6kPqEKut93iUi_QA-lazqbP09HXQKPC9TZTq1s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP188872.RAx22kZ6kPqEKut93iUi_QA-lazqbP09HXQKPC9TZTq1s130_assertion
{
miriam-gene:3614
a
ncit:C16612
.
lld:C0339525
a
ncit:C7057
.
dgn-gda:DGN42c45bb3ff334ac3f50694982c10468a
sio:SIO_000628
miriam-gene:3614
,
lld:C0339525
;
a
sio:SIO_001121
.
}
dgn-np:NP188872.RAx22kZ6kPqEKut93iUi_QA-lazqbP09HXQKPC9TZTq1s130_provenance
{
dgn-np:NP188872.RAx22kZ6kPqEKut93iUi_QA-lazqbP09HXQKPC9TZTq1s130_assertion
dcterms:description
"[Single-strand conformational analysis and PCR product sequencing were used to screen members of one family previously mapped to the RP10 locus and 47 small unmapped families with autosomal dominant retinitis pigmentosa.]. 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:10706894
;
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:NP188872.RAx22kZ6kPqEKut93iUi_QA-lazqbP09HXQKPC9TZTq1s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:43+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" .
}