@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP490815.RAy6PuaLyW7KinmCI4cPA6kV_DXNaVWsA1NH4U1zYr6qk
> .
@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:NP490815.RAy6PuaLyW7KinmCI4cPA6kV_DXNaVWsA1NH4U1zYr6qk130_head
{
this:
np:hasAssertion
dgn-np:NP490815.RAy6PuaLyW7KinmCI4cPA6kV_DXNaVWsA1NH4U1zYr6qk130_assertion
;
np:hasProvenance
dgn-np:NP490815.RAy6PuaLyW7KinmCI4cPA6kV_DXNaVWsA1NH4U1zYr6qk130_provenance
;
np:hasPublicationInfo
dgn-np:NP490815.RAy6PuaLyW7KinmCI4cPA6kV_DXNaVWsA1NH4U1zYr6qk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP490815.RAy6PuaLyW7KinmCI4cPA6kV_DXNaVWsA1NH4U1zYr6qk130_assertion
a
np:Assertion
.
dgn-np:NP490815.RAy6PuaLyW7KinmCI4cPA6kV_DXNaVWsA1NH4U1zYr6qk130_provenance
a
np:Provenance
.
dgn-np:NP490815.RAy6PuaLyW7KinmCI4cPA6kV_DXNaVWsA1NH4U1zYr6qk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP490815.RAy6PuaLyW7KinmCI4cPA6kV_DXNaVWsA1NH4U1zYr6qk130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0917713
a
ncit:C7057
.
dgn-gda:DGN619ffef9b2bd4bed7e06c3acc6e2eef8
sio:SIO_000628
miriam-gene:1756
,
lld:C0917713
;
a
sio:SIO_001121
.
}
dgn-np:NP490815.RAy6PuaLyW7KinmCI4cPA6kV_DXNaVWsA1NH4U1zYr6qk130_provenance
{
dgn-np:NP490815.RAy6PuaLyW7KinmCI4cPA6kV_DXNaVWsA1NH4U1zYr6qk130_assertion
dcterms:description
"[Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are caused in the majority of cases by deletions of the DMD gene and are readily detectable in affected males by multiplex polymerase chain reaction (PCR).]. 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:15841391
;
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:NP490815.RAy6PuaLyW7KinmCI4cPA6kV_DXNaVWsA1NH4U1zYr6qk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:27+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" .
}