@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP787603.RATiOEU8kRaTu9KUr99KjPoC25lWGE6lWoa9_bESjxL3w
> .
@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:NP787603.RATiOEU8kRaTu9KUr99KjPoC25lWGE6lWoa9_bESjxL3w130_head
{
this:
np:hasAssertion
dgn-np:NP787603.RATiOEU8kRaTu9KUr99KjPoC25lWGE6lWoa9_bESjxL3w130_assertion
;
np:hasProvenance
dgn-np:NP787603.RATiOEU8kRaTu9KUr99KjPoC25lWGE6lWoa9_bESjxL3w130_provenance
;
np:hasPublicationInfo
dgn-np:NP787603.RATiOEU8kRaTu9KUr99KjPoC25lWGE6lWoa9_bESjxL3w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP787603.RATiOEU8kRaTu9KUr99KjPoC25lWGE6lWoa9_bESjxL3w130_assertion
a
np:Assertion
.
dgn-np:NP787603.RATiOEU8kRaTu9KUr99KjPoC25lWGE6lWoa9_bESjxL3w130_provenance
a
np:Provenance
.
dgn-np:NP787603.RATiOEU8kRaTu9KUr99KjPoC25lWGE6lWoa9_bESjxL3w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP787603.RATiOEU8kRaTu9KUr99KjPoC25lWGE6lWoa9_bESjxL3w130_assertion
{
miriam-gene:25870
a
ncit:C16612
.
lld:C0013264
a
ncit:C7057
.
dgn-gda:DGNc062957b47bd865814e2baedf0939dc9
sio:SIO_000628
miriam-gene:25870
,
lld:C0013264
;
a
sio:SIO_001121
.
}
dgn-np:NP787603.RATiOEU8kRaTu9KUr99KjPoC25lWGE6lWoa9_bESjxL3w130_provenance
{
dgn-np:NP787603.RATiOEU8kRaTu9KUr99KjPoC25lWGE6lWoa9_bESjxL3w130_assertion
dcterms:description
"[These results demonstrate the applicability of PFGE for analysis of Xp21, and should facilitate the mapping of other translocations and deletions in this region, some of which lead to glycerol kinase deficiency and adrenal hypoplasia as well as DMD.]. 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:3026644
;
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:NP787603.RATiOEU8kRaTu9KUr99KjPoC25lWGE6lWoa9_bESjxL3w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:00+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" .
}