@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4
> .
@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:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_head
{
this:
np:hasAssertion
dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_assertion
;
np:hasProvenance
dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_provenance
;
np:hasPublicationInfo
dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_assertion
a
np:Assertion
.
dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_provenance
a
np:Provenance
.
dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_assertion
{
miriam-gene:25759
a
ncit:C16612
.
lld:C0013264
a
ncit:C7057
.
dgn-gda:DGNb48ab9126a4e4cb29d78df6715817270
sio:SIO_000628
miriam-gene:25759
,
lld:C0013264
;
a
sio:SIO_001121
.
}
dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_provenance
{
dgn-np:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_assertion
dcterms:description
"[Needle muscle biopsies from 14 genetically proven carriers of Duchenne muscular dystrophy (DMD), 14 possible carriers with elevated serum creatine kinase activity (SCK) and 37 possible carriers with normal SCK were compared with similar samples from 10 healthy volunteer females with the aim of identifying subtle changes that might aid carrier detection.]. 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:6452514
;
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:NP350428.RA1iizsrBGXyWLW_rQID7OhmvnvET_oopXBP5WYsSwpn4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:25+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" .
}