@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP764285.RApGKSCJBJPq2-M2Db_qtIytbYDWrgWc6Gf4JDqCkcJdY
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP764285.RApGKSCJBJPq2-M2Db_qtIytbYDWrgWc6Gf4JDqCkcJdY130_assertion
;
np:hasProvenance
dgn-np:NP764285.RApGKSCJBJPq2-M2Db_qtIytbYDWrgWc6Gf4JDqCkcJdY130_provenance
;
np:hasPublicationInfo
dgn-np:NP764285.RApGKSCJBJPq2-M2Db_qtIytbYDWrgWc6Gf4JDqCkcJdY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP764285.RApGKSCJBJPq2-M2Db_qtIytbYDWrgWc6Gf4JDqCkcJdY130_assertion
a
np:Assertion
.
dgn-np:NP764285.RApGKSCJBJPq2-M2Db_qtIytbYDWrgWc6Gf4JDqCkcJdY130_provenance
a
np:Provenance
.
dgn-np:NP764285.RApGKSCJBJPq2-M2Db_qtIytbYDWrgWc6Gf4JDqCkcJdY130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP764285.RApGKSCJBJPq2-M2Db_qtIytbYDWrgWc6Gf4JDqCkcJdY130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0263214
a
ncit:C7057
.
dgn-gda:DGN4ef6895af64796e9672565495f4abd57
sio:SIO_000628
miriam-gene:1756
,
lld:C0263214
;
a
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.
}
dgn-np:NP764285.RApGKSCJBJPq2-M2Db_qtIytbYDWrgWc6Gf4JDqCkcJdY130_provenance
{
dgn-np:NP764285.RApGKSCJBJPq2-M2Db_qtIytbYDWrgWc6Gf4JDqCkcJdY130_assertion
dcterms:description
"[In the present study, the first in the Pakistani population, frequency and distribution of deletions of 18 exons clustered in two hot spots within the dystrophin gene in 211 unrelated DMD patients were analyzed.]. 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:18353051
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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 .
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dgn-np:NP764285.RApGKSCJBJPq2-M2Db_qtIytbYDWrgWc6Gf4JDqCkcJdY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:42+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:disgenetrdf
;
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
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dgn-void:disgenetrdf
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}