@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY
> .
@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:NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_head
{
this:
np:hasAssertion
dgn-np:NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_assertion
;
np:hasProvenance
dgn-np:NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_provenance
;
np:hasPublicationInfo
dgn-np:NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_assertion
a
np:Assertion
.
dgn-np:NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_provenance
a
np:Provenance
.
dgn-np:NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_assertion
{
miriam-gene:8859
a
ncit:C16612
.
lld:C0339525
a
ncit:C7057
.
dgn-gda:DGNa073b6daba9836f510308365fedc434e
sio:SIO_000628
miriam-gene:8859
,
lld:C0339525
;
a
sio:SIO_001121
.
}
dgn-np:NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_provenance
{
dgn-np:NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_assertion
dcterms:description
"[To examine the role of RP1 mutations in RP, we screened 101 unrelated Chinese RP patients (unselected for mode of inheritance) and 190 elderly normal control subjects for sequence changes in the coding exons for the 2156 amino acid RP1 protein.]. 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:11317367
;
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:NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:08+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" .
}