@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE
> .
@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:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_head
{
this:
np:hasAssertion
dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_assertion
;
np:hasProvenance
dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance
;
np:hasPublicationInfo
dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_assertion
a
np:Assertion
.
dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance
a
np:Provenance
.
dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0026850
a
ncit:C7057
.
dgn-gda:DGNe3141115469118561169f18db9a70952
sio:SIO_000628
miriam-gene:1756
,
lld:C0026850
;
a
sio:SIO_001121
.
}
dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_provenance
{
dgn-np:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_assertion
dcterms:description
"[Somatic cell testing of dystrophin expression may offer an alternative to established genetic carrier tests for those women in whom deletions of the DMD are not detectable, whose pedigree structure does not permit linkage analysis, or in whom standard phenotypic analyses are ambiguous.]. 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:2658563
;
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:NP1295593.RA7Wh8PE4FgRu80-7wMp69QD7Rd42odMW6exfTat3v5gE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:33+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" .
}