@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE
> .
@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:NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_head
{
this:
np:hasAssertion
dgn-np:NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_assertion
;
np:hasProvenance
dgn-np:NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_provenance
;
np:hasPublicationInfo
dgn-np:NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_assertion
a
np:Assertion
.
dgn-np:NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_provenance
a
np:Provenance
.
dgn-np:NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_assertion
{
miriam-gene:8087
a
ncit:C16612
.
lld:C0026848
a
ncit:C7057
.
dgn-gda:DGN5ee57227202af864dcd31254a1bea459
sio:SIO_000628
miriam-gene:8087
,
lld:C0026848
;
a
sio:SIO_001121
.
}
dgn-np:NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_provenance
{
dgn-np:NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_assertion
dcterms:description
"[Since facioscapulohumeral muscular dystrophy (FSHD) is an inherited myopathy characterised by altered splicing of mRNAs encoding muscle specific proteins, we have studied the splicing pattern of FXR1 mRNA in myoblasts and myotubes of FSHD patients.]. 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:18628314
;
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:NP427772.RABIQAOlEeZJojPTYqWMlAiMG7NKVjmD0KmZgIHsYfYDE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:13+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" .
}