@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP538935.RAgdAlqAN-v2wOuwBarbjjDTfyZLG5wTfIJvceWUu6Y2c
> .
@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#
> .
dgn-np:NP538935.RAgdAlqAN-v2wOuwBarbjjDTfyZLG5wTfIJvceWUu6Y2c130_head
{
this:
np:hasAssertion
dgn-np:NP538935.RAgdAlqAN-v2wOuwBarbjjDTfyZLG5wTfIJvceWUu6Y2c130_assertion
;
np:hasProvenance
dgn-np:NP538935.RAgdAlqAN-v2wOuwBarbjjDTfyZLG5wTfIJvceWUu6Y2c130_provenance
;
np:hasPublicationInfo
dgn-np:NP538935.RAgdAlqAN-v2wOuwBarbjjDTfyZLG5wTfIJvceWUu6Y2c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP538935.RAgdAlqAN-v2wOuwBarbjjDTfyZLG5wTfIJvceWUu6Y2c130_assertion
a
np:Assertion
.
dgn-np:NP538935.RAgdAlqAN-v2wOuwBarbjjDTfyZLG5wTfIJvceWUu6Y2c130_provenance
a
np:Provenance
.
dgn-np:NP538935.RAgdAlqAN-v2wOuwBarbjjDTfyZLG5wTfIJvceWUu6Y2c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP538935.RAgdAlqAN-v2wOuwBarbjjDTfyZLG5wTfIJvceWUu6Y2c130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0022821
a
ncit:C7057
.
dgn-gda:DGNc6db353ab2af7e3247c52b462d7b8e0e
sio:SIO_000628
miriam-gene:1756
,
lld:C0022821
;
a
sio:SIO_001121
.
}
dgn-np:NP538935.RAgdAlqAN-v2wOuwBarbjjDTfyZLG5wTfIJvceWUu6Y2c130_provenance
{
dgn-np:NP538935.RAgdAlqAN-v2wOuwBarbjjDTfyZLG5wTfIJvceWUu6Y2c130_assertion
dcterms:description
"[These mice show many pathologic and phenotypic signs typical of DMD in humans including kyphosis and shorter life span, all of which are not seen in the mdx mice due to their utrophin upregulation that partially compensates the loss of dystrophin functions and leads to mild phenotypes.]. 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:18973234
;
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:NP538935.RAgdAlqAN-v2wOuwBarbjjDTfyZLG5wTfIJvceWUu6Y2c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}