@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP844722.RAhRczA1iPbtmyUVBuZjv5wYcxmF3S9QKUeSRN3HcAeEk
> .
@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:NP844722.RAhRczA1iPbtmyUVBuZjv5wYcxmF3S9QKUeSRN3HcAeEk130_head
{
this:
np:hasAssertion
dgn-np:NP844722.RAhRczA1iPbtmyUVBuZjv5wYcxmF3S9QKUeSRN3HcAeEk130_assertion
;
np:hasProvenance
dgn-np:NP844722.RAhRczA1iPbtmyUVBuZjv5wYcxmF3S9QKUeSRN3HcAeEk130_provenance
;
np:hasPublicationInfo
dgn-np:NP844722.RAhRczA1iPbtmyUVBuZjv5wYcxmF3S9QKUeSRN3HcAeEk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP844722.RAhRczA1iPbtmyUVBuZjv5wYcxmF3S9QKUeSRN3HcAeEk130_assertion
a
np:Assertion
.
dgn-np:NP844722.RAhRczA1iPbtmyUVBuZjv5wYcxmF3S9QKUeSRN3HcAeEk130_provenance
a
np:Provenance
.
dgn-np:NP844722.RAhRczA1iPbtmyUVBuZjv5wYcxmF3S9QKUeSRN3HcAeEk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP844722.RAhRczA1iPbtmyUVBuZjv5wYcxmF3S9QKUeSRN3HcAeEk130_assertion
{
miriam-gene:760
a
ncit:C16612
.
lld:C0029454
a
ncit:C7057
.
dgn-gda:DGNcaf5f6090d7d71cbb861bd92e0abb47f
sio:SIO_000628
miriam-gene:760
,
lld:C0029454
;
a
sio:SIO_001121
.
}
dgn-np:NP844722.RAhRczA1iPbtmyUVBuZjv5wYcxmF3S9QKUeSRN3HcAeEk130_provenance
{
dgn-np:NP844722.RAhRczA1iPbtmyUVBuZjv5wYcxmF3S9QKUeSRN3HcAeEk130_assertion
dcterms:description
"[Confirmation of clinical diagnosis by molecular methods is essential as the clinical features of the CAII deficiency syndrome are similar to other forms of OP but the treatment modalities are different.]. 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:20935402
;
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:NP844722.RAhRczA1iPbtmyUVBuZjv5wYcxmF3S9QKUeSRN3HcAeEk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:07+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" .
}