@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP864710.RAncfCyg8VbOVClQfxQAdxl6UhnB1-K38h2WLk0_pKr9k
> .
@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/
> .
@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:NP864710.RAncfCyg8VbOVClQfxQAdxl6UhnB1-K38h2WLk0_pKr9k130_head
{
this:
np:hasAssertion
dgn-np:NP864710.RAncfCyg8VbOVClQfxQAdxl6UhnB1-K38h2WLk0_pKr9k130_assertion
;
np:hasProvenance
dgn-np:NP864710.RAncfCyg8VbOVClQfxQAdxl6UhnB1-K38h2WLk0_pKr9k130_provenance
;
np:hasPublicationInfo
dgn-np:NP864710.RAncfCyg8VbOVClQfxQAdxl6UhnB1-K38h2WLk0_pKr9k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP864710.RAncfCyg8VbOVClQfxQAdxl6UhnB1-K38h2WLk0_pKr9k130_assertion
a
np:Assertion
.
dgn-np:NP864710.RAncfCyg8VbOVClQfxQAdxl6UhnB1-K38h2WLk0_pKr9k130_provenance
a
np:Provenance
.
dgn-np:NP864710.RAncfCyg8VbOVClQfxQAdxl6UhnB1-K38h2WLk0_pKr9k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP864710.RAncfCyg8VbOVClQfxQAdxl6UhnB1-K38h2WLk0_pKr9k130_assertion
{
miriam-gene:57096
a
ncit:C16612
.
lld:C0017601
a
ncit:C7057
.
dgn-gda:DGN3d4b9548988e4d4e7e065af19cd85010
sio:SIO_000628
miriam-gene:57096
,
lld:C0017601
;
a
sio:SIO_001121
.
}
dgn-np:NP864710.RAncfCyg8VbOVClQfxQAdxl6UhnB1-K38h2WLk0_pKr9k130_provenance
{
dgn-np:NP864710.RAncfCyg8VbOVClQfxQAdxl6UhnB1-K38h2WLk0_pKr9k130_assertion
dcterms:description
"[Altogether, the data support that heterozygous non-synonymous variants of RPGRIP1 may cause or increase the susceptibility to various forms of glaucoma and that among other factors, physical impairment of the interaction of RPGRIP1with different proteins may contribute to the pathogenesis of forms of glaucoma.]. 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:21224891
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP864710.RAncfCyg8VbOVClQfxQAdxl6UhnB1-K38h2WLk0_pKr9k130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:16+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" .
}