@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k
> .
@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/v4.0.0/void/
> .
dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_head
{
this:
np:hasAssertion
dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_assertion
;
np:hasProvenance
dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_provenance
;
np:hasPublicationInfo
dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_assertion
a
np:Assertion
.
dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_provenance
a
np:Provenance
.
dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_assertion
{
miriam-gene:7439
a
ncit:C16612
.
lld:C0917713
a
ncit:C7057
.
dgn-gda:DGNafa15dd4031dc53bfb034cfcf9efbcd2
sio:SIO_000628
miriam-gene:7439
,
lld:C0917713
;
a
sio:SIO_001121
.
}
dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_provenance
{
dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_assertion
dcterms:description
"[The aim of this study was to identify point mutations in patients with Duchenne or Becker muscular dystrophy (DMD or BMD) who have no gross DNA rearrangements detectable by Southern blot analysis or multiplex exon amplification.]. 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:8257990
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:52+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}