@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso
> .
@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:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_head
{
this:
np:hasAssertion
dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_assertion
;
np:hasProvenance
dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_provenance
;
np:hasPublicationInfo
dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_assertion
a
np:Assertion
.
dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_provenance
a
np:Provenance
.
dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0339510
a
ncit:C7057
.
dgn-gda:DGN2454eabaa3685be58cb281a28707cdea
sio:SIO_000628
miriam-gene:1756
,
lld:C0339510
;
a
sio:SIO_001121
.
}
dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_provenance
{
dgn-np:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_assertion
dcterms:description
"[Estimating carrier risks for female relatives of Duchenne (DMD) and Becker (BMD) dystrophy sufferers depends upon calculation of segregational risks, supplemented by enzyme tests which show considerable overlap between carrier and control data.]. 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:2688825
;
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:NP184390.RAUzEEJMc_m5PvDGrtxugRxbc_X2CrmsPu7g4JS5vdkso130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:39+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" .
}