@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP810846.RA74s9K0BFN-q6TDWBf1VjeYox9WeLCWx3nvwJn7aD5vI
> .
@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:NP810846.RA74s9K0BFN-q6TDWBf1VjeYox9WeLCWx3nvwJn7aD5vI130_head
{
this:
np:hasAssertion
dgn-np:NP810846.RA74s9K0BFN-q6TDWBf1VjeYox9WeLCWx3nvwJn7aD5vI130_assertion
;
np:hasProvenance
dgn-np:NP810846.RA74s9K0BFN-q6TDWBf1VjeYox9WeLCWx3nvwJn7aD5vI130_provenance
;
np:hasPublicationInfo
dgn-np:NP810846.RA74s9K0BFN-q6TDWBf1VjeYox9WeLCWx3nvwJn7aD5vI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP810846.RA74s9K0BFN-q6TDWBf1VjeYox9WeLCWx3nvwJn7aD5vI130_assertion
a
np:Assertion
.
dgn-np:NP810846.RA74s9K0BFN-q6TDWBf1VjeYox9WeLCWx3nvwJn7aD5vI130_provenance
a
np:Provenance
.
dgn-np:NP810846.RA74s9K0BFN-q6TDWBf1VjeYox9WeLCWx3nvwJn7aD5vI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP810846.RA74s9K0BFN-q6TDWBf1VjeYox9WeLCWx3nvwJn7aD5vI130_assertion
{
miriam-gene:4151
a
ncit:C16612
.
lld:C0013264
a
ncit:C7057
.
dgn-gda:DGNafcfb5122e07083c36f9e91ba02f6f45
sio:SIO_000628
miriam-gene:4151
,
lld:C0013264
;
a
sio:SIO_001121
.
}
dgn-np:NP810846.RA74s9K0BFN-q6TDWBf1VjeYox9WeLCWx3nvwJn7aD5vI130_provenance
{
dgn-np:NP810846.RA74s9K0BFN-q6TDWBf1VjeYox9WeLCWx3nvwJn7aD5vI130_assertion
dcterms:description
"[Serum creatine kinase, myoglobin, and percentage lymphocyte capping was determined in ten patients with Duchenne muscular dystrophy, 12 carriers (nine definite and three probable), 16 other female relatives, and eight normal controls.]. 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:7401126
;
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:NP810846.RA74s9K0BFN-q6TDWBf1VjeYox9WeLCWx3nvwJn7aD5vI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:17+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" .
}