@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP880225.RAPES5GF4L-1DVqRygcPH6wauAeoV2NE1mTONdujhfeZc
> .
@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:NP880225.RAPES5GF4L-1DVqRygcPH6wauAeoV2NE1mTONdujhfeZc130_head
{
this:
np:hasAssertion
dgn-np:NP880225.RAPES5GF4L-1DVqRygcPH6wauAeoV2NE1mTONdujhfeZc130_assertion
;
np:hasProvenance
dgn-np:NP880225.RAPES5GF4L-1DVqRygcPH6wauAeoV2NE1mTONdujhfeZc130_provenance
;
np:hasPublicationInfo
dgn-np:NP880225.RAPES5GF4L-1DVqRygcPH6wauAeoV2NE1mTONdujhfeZc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP880225.RAPES5GF4L-1DVqRygcPH6wauAeoV2NE1mTONdujhfeZc130_assertion
a
np:Assertion
.
dgn-np:NP880225.RAPES5GF4L-1DVqRygcPH6wauAeoV2NE1mTONdujhfeZc130_provenance
a
np:Provenance
.
dgn-np:NP880225.RAPES5GF4L-1DVqRygcPH6wauAeoV2NE1mTONdujhfeZc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP880225.RAPES5GF4L-1DVqRygcPH6wauAeoV2NE1mTONdujhfeZc130_assertion
{
miriam-gene:1605
a
ncit:C16612
.
lld:C0206656
a
ncit:C7057
.
dgn-gda:DGNb4b18acfc35972ca9cb9ff6120b92a7e
sio:SIO_000628
miriam-gene:1605
,
lld:C0206656
;
a
sio:SIO_001121
.
}
dgn-np:NP880225.RAPES5GF4L-1DVqRygcPH6wauAeoV2NE1mTONdujhfeZc130_provenance
{
dgn-np:NP880225.RAPES5GF4L-1DVqRygcPH6wauAeoV2NE1mTONdujhfeZc130_assertion
dcterms:description
"[Expression of natively glycosylated alpha dystroglycan and alpha sarcoglycan was reduced in mdx RMS, whereas dystrophin expression was absent in almost all human RMS, both for embryonal and alveolar RMS subtypes.]. 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:20019182
;
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:NP880225.RAPES5GF4L-1DVqRygcPH6wauAeoV2NE1mTONdujhfeZc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:58+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" .
}