@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1102481.RA606ZTi2uPTJrEs1ZxwH_wpRJuTIWuX07RPFUyiNcHPY
> .
@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:NP1102481.RA606ZTi2uPTJrEs1ZxwH_wpRJuTIWuX07RPFUyiNcHPY130_head
{
this:
np:hasAssertion
dgn-np:NP1102481.RA606ZTi2uPTJrEs1ZxwH_wpRJuTIWuX07RPFUyiNcHPY130_assertion
;
np:hasProvenance
dgn-np:NP1102481.RA606ZTi2uPTJrEs1ZxwH_wpRJuTIWuX07RPFUyiNcHPY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1102481.RA606ZTi2uPTJrEs1ZxwH_wpRJuTIWuX07RPFUyiNcHPY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1102481.RA606ZTi2uPTJrEs1ZxwH_wpRJuTIWuX07RPFUyiNcHPY130_assertion
a
np:Assertion
.
dgn-np:NP1102481.RA606ZTi2uPTJrEs1ZxwH_wpRJuTIWuX07RPFUyiNcHPY130_provenance
a
np:Provenance
.
dgn-np:NP1102481.RA606ZTi2uPTJrEs1ZxwH_wpRJuTIWuX07RPFUyiNcHPY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1102481.RA606ZTi2uPTJrEs1ZxwH_wpRJuTIWuX07RPFUyiNcHPY130_assertion
{
miriam-gene:1120
a
ncit:C16612
.
lld:C0699743
a
ncit:C7057
.
dgn-gda:DGN25dd908f7fa33b655f41ce3c3e00fcc3
sio:SIO_000628
miriam-gene:1120
,
lld:C0699743
;
a
sio:SIO_001121
.
}
dgn-np:NP1102481.RA606ZTi2uPTJrEs1ZxwH_wpRJuTIWuX07RPFUyiNcHPY130_provenance
{
dgn-np:NP1102481.RA606ZTi2uPTJrEs1ZxwH_wpRJuTIWuX07RPFUyiNcHPY130_assertion
dcterms:description
"[Since our report of CHKB mutations found in 15 cases with megaconial congenital muscular dystrophy from Japanese, Turkish, and British populations, we have further identified two British and one French patients.]. 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:23945283
;
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:NP1102481.RA606ZTi2uPTJrEs1ZxwH_wpRJuTIWuX07RPFUyiNcHPY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:05+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" .
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pav:version
"v4.0.0" .
}