@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP879210.RAvnp2emkcgwI9YhtcdOBqvF10jPp1d0h1A9E1FVomY7Y
> .
@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:NP879210.RAvnp2emkcgwI9YhtcdOBqvF10jPp1d0h1A9E1FVomY7Y130_head
{
this:
np:hasAssertion
dgn-np:NP879210.RAvnp2emkcgwI9YhtcdOBqvF10jPp1d0h1A9E1FVomY7Y130_assertion
;
np:hasProvenance
dgn-np:NP879210.RAvnp2emkcgwI9YhtcdOBqvF10jPp1d0h1A9E1FVomY7Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP879210.RAvnp2emkcgwI9YhtcdOBqvF10jPp1d0h1A9E1FVomY7Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP879210.RAvnp2emkcgwI9YhtcdOBqvF10jPp1d0h1A9E1FVomY7Y130_assertion
a
np:Assertion
.
dgn-np:NP879210.RAvnp2emkcgwI9YhtcdOBqvF10jPp1d0h1A9E1FVomY7Y130_provenance
a
np:Provenance
.
dgn-np:NP879210.RAvnp2emkcgwI9YhtcdOBqvF10jPp1d0h1A9E1FVomY7Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP879210.RAvnp2emkcgwI9YhtcdOBqvF10jPp1d0h1A9E1FVomY7Y130_assertion
{
miriam-gene:7439
a
ncit:C16612
.
lld:C3542021
a
ncit:C7057
.
dgn-gda:DGN8183f5867d75a8688c0b4cd84ac34b4d
sio:SIO_000628
miriam-gene:7439
,
lld:C3542021
;
a
sio:SIO_001121
.
}
dgn-np:NP879210.RAvnp2emkcgwI9YhtcdOBqvF10jPp1d0h1A9E1FVomY7Y130_provenance
{
dgn-np:NP879210.RAvnp2emkcgwI9YhtcdOBqvF10jPp1d0h1A9E1FVomY7Y130_assertion
dcterms:description
"[Duchenne and Becker muscular dystrophy (DMD and BMD, respectively) are allelic disorders with different clinical presentations and severity determined by mutations in the gene DMD, which encodes the sarcolemmal protein dystrophin.]. 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:21399986
;
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:NP879210.RAvnp2emkcgwI9YhtcdOBqvF10jPp1d0h1A9E1FVomY7Y130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:23+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" .
}