@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q
> .
@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:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_head
{
this:
np:hasAssertion
dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_assertion
;
np:hasProvenance
dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_assertion
a
np:Assertion
.
dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_provenance
a
np:Provenance
.
dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0041408
a
ncit:C7057
.
dgn-gda:DGN1669f8cf038a888fd80edfbda7eba94f
sio:SIO_000628
miriam-gene:1756
,
lld:C0041408
;
a
sio:SIO_001121
.
}
dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_provenance
{
dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_assertion
dcterms:description
"[Neither female Duchenne muscular dystrophy (DMD) nor BMD due to homozygous dystrophin mutation has ever been identified although female DMD has been found in patients with Turner syndrome or unilateral parental disomy for X chromosome.]. 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:19396825
;
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:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:42+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" .
}