@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP426697.RA8QBsLeqN3lts_nK2H6Wh5f-PUY6wvu4M9kx3RSrBFA4
> .
@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/v3.0.0/void/
> .
dgn-np:NP426697.RA8QBsLeqN3lts_nK2H6Wh5f-PUY6wvu4M9kx3RSrBFA4130_head
{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP426697.RA8QBsLeqN3lts_nK2H6Wh5f-PUY6wvu4M9kx3RSrBFA4130_assertion
a
np:Assertion
.
dgn-np:NP426697.RA8QBsLeqN3lts_nK2H6Wh5f-PUY6wvu4M9kx3RSrBFA4130_provenance
a
np:Provenance
.
dgn-np:NP426697.RA8QBsLeqN3lts_nK2H6Wh5f-PUY6wvu4M9kx3RSrBFA4130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:2710
a
ncit:C16612
.
lld:C0013264
a
ncit:C7057
.
dgn-gda:DGN9ec0ef562a4684d7121170086d5c34a1
sio:SIO_000628
miriam-gene:2710
,
lld:C0013264
;
a
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.
}
dgn-np:NP426697.RA8QBsLeqN3lts_nK2H6Wh5f-PUY6wvu4M9kx3RSrBFA4130_provenance
{
dgn-np:NP426697.RA8QBsLeqN3lts_nK2H6Wh5f-PUY6wvu4M9kx3RSrBFA4130_assertion
dcterms:description
"[We developed a pair of yeast artificial chromosome (YAC) contigs spanning at least 1.2 Mb and encompassing the region from the telomeric end of the Duchenne muscular dystrophy (DMD) locus to beyond YHX39 (DXS727), including the genes for AHC and GK.]. 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:8314578
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP426697.RA8QBsLeqN3lts_nK2H6Wh5f-PUY6wvu4M9kx3RSrBFA4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:48+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
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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