@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP355647.RAc5gPLfdqXcMmfOF3RkvdXHWFt1LgC21GUoVIvqneUEI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP355647.RAc5gPLfdqXcMmfOF3RkvdXHWFt1LgC21GUoVIvqneUEI130_head
{
this:
np:hasAssertion
dgn-np:NP355647.RAc5gPLfdqXcMmfOF3RkvdXHWFt1LgC21GUoVIvqneUEI130_assertion
;
np:hasProvenance
dgn-np:NP355647.RAc5gPLfdqXcMmfOF3RkvdXHWFt1LgC21GUoVIvqneUEI130_provenance
;
np:hasPublicationInfo
dgn-np:NP355647.RAc5gPLfdqXcMmfOF3RkvdXHWFt1LgC21GUoVIvqneUEI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP355647.RAc5gPLfdqXcMmfOF3RkvdXHWFt1LgC21GUoVIvqneUEI130_assertion
a
np:Assertion
.
dgn-np:NP355647.RAc5gPLfdqXcMmfOF3RkvdXHWFt1LgC21GUoVIvqneUEI130_provenance
a
np:Provenance
.
dgn-np:NP355647.RAc5gPLfdqXcMmfOF3RkvdXHWFt1LgC21GUoVIvqneUEI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP355647.RAc5gPLfdqXcMmfOF3RkvdXHWFt1LgC21GUoVIvqneUEI130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C1533847
a
ncit:C7057
.
dgn-gda:DGN5b89ea501273d7b3c6d4333a59a2fca9
sio:SIO_000628
miriam-gene:1756
,
lld:C1533847
;
a
sio:SIO_001122
.
}
dgn-np:NP355647.RAc5gPLfdqXcMmfOF3RkvdXHWFt1LgC21GUoVIvqneUEI130_provenance
{
dgn-np:NP355647.RAc5gPLfdqXcMmfOF3RkvdXHWFt1LgC21GUoVIvqneUEI130_assertion
dcterms:description
"[The first comprehensive mutation scanning of the exons and splice junctions of the dystrophin gene in patients with sporadic DCM presents the evidence that point mutations are associated with sporadic DCM without clinical evidence of skeletal myopathy.]. 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:12359139
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP355647.RAc5gPLfdqXcMmfOF3RkvdXHWFt1LgC21GUoVIvqneUEI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:05+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}