@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ
> .
@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 np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_head
{
this:
np:hasAssertion
dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_assertion
;
np:hasProvenance
dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_assertion
a
np:Assertion
.
dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_provenance
a
np:Provenance
.
dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_assertion
{
miriam-gene:56172
a
ncit:C16612
.
lld:C0856830
a
ncit:C7057
.
dgn-gda:DGNf267c30cfcacfa8eb0aad356b7ddc1f2
sio:SIO_000628
miriam-gene:56172
,
lld:C0856830
;
a
sio:SIO_001122
.
}
dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_provenance
{
dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_assertion
dct:description
"[These observations represent the fourth and fifth families with heritable CPPD whose disease phenotypes are linked to the CCAL2 locus and who have missense mutations in the amino terminus of ANKH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:13130483
;
prov:wasDerivedFrom
dgn-void:uniprot-2016
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
dgn-void:uniprot-2016
pav:importedOn
"2016-01-25"^^
xsd:date
.
}
dgn-np:NP2918.RABJYXmiXTc0kKjPIZEHudjlEQmzwag_e4b8QGBqJ-2OQ130_publicationInfo
{
this:
dct:created
"2016-05-13T12:41:51+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct: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" .
}