@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE
> .
@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:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_head
{
this:
np:hasAssertion
dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_assertion
;
np:hasProvenance
dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_provenance
;
np:hasPublicationInfo
dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_assertion
a
np:Assertion
.
dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_provenance
a
np:Provenance
.
dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_assertion
{
miriam-gene:6445
a
ncit:C16612
.
lld:C2936331
a
ncit:C7057
.
dgn-gda:DGNb844f93ee1075f6aa48449fa9c275cfd
sio:SIO_000628
miriam-gene:6445
,
lld:C2936331
;
a
sio:SIO_001122
.
}
dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_provenance
{
dgn-np:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_assertion
dcterms:description
"[This study, the first mutational analysis of Indian patients with sarcoglycanopathies suggests gamma SG mutations were the most common and the most prevalent mutation in the gamma SG gene was 525del T.]. 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:19770540
;
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:NP692518.RAsUyALPY4_l4mlAhvu-xn7e9dTKT3IpIWyXYRkYz-XaE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:37+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" .
}