@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP667239.RAGIyLKnSSerCBe8sBA_4oCODoZNIjh9k8ifWGbahNzvo
> .
@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:NP667239.RAGIyLKnSSerCBe8sBA_4oCODoZNIjh9k8ifWGbahNzvo130_head
{
this:
np:hasAssertion
dgn-np:NP667239.RAGIyLKnSSerCBe8sBA_4oCODoZNIjh9k8ifWGbahNzvo130_assertion
;
np:hasProvenance
dgn-np:NP667239.RAGIyLKnSSerCBe8sBA_4oCODoZNIjh9k8ifWGbahNzvo130_provenance
;
np:hasPublicationInfo
dgn-np:NP667239.RAGIyLKnSSerCBe8sBA_4oCODoZNIjh9k8ifWGbahNzvo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP667239.RAGIyLKnSSerCBe8sBA_4oCODoZNIjh9k8ifWGbahNzvo130_assertion
a
np:Assertion
.
dgn-np:NP667239.RAGIyLKnSSerCBe8sBA_4oCODoZNIjh9k8ifWGbahNzvo130_provenance
a
np:Provenance
.
dgn-np:NP667239.RAGIyLKnSSerCBe8sBA_4oCODoZNIjh9k8ifWGbahNzvo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP667239.RAGIyLKnSSerCBe8sBA_4oCODoZNIjh9k8ifWGbahNzvo130_assertion
{
miriam-gene:5367
a
ncit:C16612
.
lld:C0015397
a
ncit:C7057
.
dgn-gda:DGN796a880f9c51c64c7dabb94261b240df
sio:SIO_000628
miriam-gene:5367
,
lld:C0015397
;
a
sio:SIO_001121
.
}
dgn-np:NP667239.RAGIyLKnSSerCBe8sBA_4oCODoZNIjh9k8ifWGbahNzvo130_provenance
{
dgn-np:NP667239.RAGIyLKnSSerCBe8sBA_4oCODoZNIjh9k8ifWGbahNzvo130_assertion
dcterms:description
"[A large family with multiple individuals affected by autosomal recessive retinitis pigmentosa was ascertained in the Punjab province of Pakistan as part of an ongoing project between the CEMB, Lahore, Pakistan and the NEI to identify genetic causes of eye diseases.]. 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:15570217
;
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:NP667239.RAGIyLKnSSerCBe8sBA_4oCODoZNIjh9k8ifWGbahNzvo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:43+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" .
}