@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP280334.RAu8Qi89uVn0W_HO07leKvFmzLUAuxXGbKh1IFpA_oYcg
> .
@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/v3.0.0/void/
> .
dgn-np:NP280334.RAu8Qi89uVn0W_HO07leKvFmzLUAuxXGbKh1IFpA_oYcg130_head
{
this:
np:hasAssertion
dgn-np:NP280334.RAu8Qi89uVn0W_HO07leKvFmzLUAuxXGbKh1IFpA_oYcg130_assertion
;
np:hasProvenance
dgn-np:NP280334.RAu8Qi89uVn0W_HO07leKvFmzLUAuxXGbKh1IFpA_oYcg130_provenance
;
np:hasPublicationInfo
dgn-np:NP280334.RAu8Qi89uVn0W_HO07leKvFmzLUAuxXGbKh1IFpA_oYcg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP280334.RAu8Qi89uVn0W_HO07leKvFmzLUAuxXGbKh1IFpA_oYcg130_assertion
a
np:Assertion
.
dgn-np:NP280334.RAu8Qi89uVn0W_HO07leKvFmzLUAuxXGbKh1IFpA_oYcg130_provenance
a
np:Provenance
.
dgn-np:NP280334.RAu8Qi89uVn0W_HO07leKvFmzLUAuxXGbKh1IFpA_oYcg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP280334.RAu8Qi89uVn0W_HO07leKvFmzLUAuxXGbKh1IFpA_oYcg130_assertion
{
miriam-gene:825
a
ncit:C16612
.
lld:C0026850
a
ncit:C7057
.
dgn-gda:DGN0890ad737dbf96b12fe3a3c8a8ba9044
sio:SIO_000628
miriam-gene:825
,
lld:C0026850
;
a
sio:SIO_001121
.
}
dgn-np:NP280334.RAu8Qi89uVn0W_HO07leKvFmzLUAuxXGbKh1IFpA_oYcg130_provenance
{
dgn-np:NP280334.RAu8Qi89uVn0W_HO07leKvFmzLUAuxXGbKh1IFpA_oYcg130_assertion
dcterms:description
"[These data indicate that muscular dystrophy caused by mutations in CANP3 are found in patients from all countries examined so far and further support the wide heterogeneity of molecular defects in this rare disease.]. 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:9150160
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP280334.RAu8Qi89uVn0W_HO07leKvFmzLUAuxXGbKh1IFpA_oYcg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:20+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}