@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP592581.RA8pYjAKXgqqw1B9qKHyWq-CxXbBUW-snx3V3-MPFT0Wc
> .
@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
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;
np:hasProvenance
dgn-np:NP592581.RA8pYjAKXgqqw1B9qKHyWq-CxXbBUW-snx3V3-MPFT0Wc130_provenance
;
np:hasPublicationInfo
dgn-np:NP592581.RA8pYjAKXgqqw1B9qKHyWq-CxXbBUW-snx3V3-MPFT0Wc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP592581.RA8pYjAKXgqqw1B9qKHyWq-CxXbBUW-snx3V3-MPFT0Wc130_assertion
a
np:Assertion
.
dgn-np:NP592581.RA8pYjAKXgqqw1B9qKHyWq-CxXbBUW-snx3V3-MPFT0Wc130_provenance
a
np:Provenance
.
dgn-np:NP592581.RA8pYjAKXgqqw1B9qKHyWq-CxXbBUW-snx3V3-MPFT0Wc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP592581.RA8pYjAKXgqqw1B9qKHyWq-CxXbBUW-snx3V3-MPFT0Wc130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C1883552
a
ncit:C7057
.
dgn-gda:DGN48b6bba1e20b2fd609d9115a3b75b872
sio:SIO_000628
miriam-gene:1756
,
lld:C1883552
;
a
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.
}
dgn-np:NP592581.RA8pYjAKXgqqw1B9qKHyWq-CxXbBUW-snx3V3-MPFT0Wc130_provenance
{
dgn-np:NP592581.RA8pYjAKXgqqw1B9qKHyWq-CxXbBUW-snx3V3-MPFT0Wc130_assertion
dcterms:description
"[Our results show that analysis of dystrophin expression is useful for the differential diagnosis of carriers of Xp21 dystrophy and autosomal muscular dystrophy, but that dystrophin expression does not correlate directly with the degree of clinical weakness.]. 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:8358239
;
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 .
}
dgn-np:NP592581.RA8pYjAKXgqqw1B9qKHyWq-CxXbBUW-snx3V3-MPFT0Wc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:56+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
> , <
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> , <
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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"v2.1.0" .
}