@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP524913.RA1CGFFVUeYAodtF9-8yZjaxSRm2_BmYQfN8Ledetr3Oc
> .
@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:NP524913.RA1CGFFVUeYAodtF9-8yZjaxSRm2_BmYQfN8Ledetr3Oc130_head
{
this:
np:hasAssertion
dgn-np:NP524913.RA1CGFFVUeYAodtF9-8yZjaxSRm2_BmYQfN8Ledetr3Oc130_assertion
;
np:hasProvenance
dgn-np:NP524913.RA1CGFFVUeYAodtF9-8yZjaxSRm2_BmYQfN8Ledetr3Oc130_provenance
;
np:hasPublicationInfo
dgn-np:NP524913.RA1CGFFVUeYAodtF9-8yZjaxSRm2_BmYQfN8Ledetr3Oc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP524913.RA1CGFFVUeYAodtF9-8yZjaxSRm2_BmYQfN8Ledetr3Oc130_assertion
a
np:Assertion
.
dgn-np:NP524913.RA1CGFFVUeYAodtF9-8yZjaxSRm2_BmYQfN8Ledetr3Oc130_provenance
a
np:Provenance
.
dgn-np:NP524913.RA1CGFFVUeYAodtF9-8yZjaxSRm2_BmYQfN8Ledetr3Oc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP524913.RA1CGFFVUeYAodtF9-8yZjaxSRm2_BmYQfN8Ledetr3Oc130_assertion
{
miriam-gene:1736
a
ncit:C16612
.
lld:C1148551
a
ncit:C7057
.
dgn-gda:DGNbc77e819f67f85320ccdac064afebd39
sio:SIO_000628
miriam-gene:1736
,
lld:C1148551
;
a
sio:SIO_001121
.
}
dgn-np:NP524913.RA1CGFFVUeYAodtF9-8yZjaxSRm2_BmYQfN8Ledetr3Oc130_provenance
{
dgn-np:NP524913.RA1CGFFVUeYAodtF9-8yZjaxSRm2_BmYQfN8Ledetr3Oc130_assertion
dcterms:description
"[We report the precise mapping and characterization of the genomic structure of the human homolog of the rat gene for the nucleolar protein NAP57, which has been reported to be responsible for X-linked dyskeratosis congenita (DKC).]. 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:9888995
;
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:NP524913.RA1CGFFVUeYAodtF9-8yZjaxSRm2_BmYQfN8Ledetr3Oc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:15+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" .
}