@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP928443.RAHUXdUYSbxQCG78kd263sUrop5W4Gpn1k9CTufVlnSRg
> .
@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:NP928443.RAHUXdUYSbxQCG78kd263sUrop5W4Gpn1k9CTufVlnSRg130_head
{
this:
np:hasAssertion
dgn-np:NP928443.RAHUXdUYSbxQCG78kd263sUrop5W4Gpn1k9CTufVlnSRg130_assertion
;
np:hasProvenance
dgn-np:NP928443.RAHUXdUYSbxQCG78kd263sUrop5W4Gpn1k9CTufVlnSRg130_provenance
;
np:hasPublicationInfo
dgn-np:NP928443.RAHUXdUYSbxQCG78kd263sUrop5W4Gpn1k9CTufVlnSRg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP928443.RAHUXdUYSbxQCG78kd263sUrop5W4Gpn1k9CTufVlnSRg130_assertion
a
np:Assertion
.
dgn-np:NP928443.RAHUXdUYSbxQCG78kd263sUrop5W4Gpn1k9CTufVlnSRg130_provenance
a
np:Provenance
.
dgn-np:NP928443.RAHUXdUYSbxQCG78kd263sUrop5W4Gpn1k9CTufVlnSRg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP928443.RAHUXdUYSbxQCG78kd263sUrop5W4Gpn1k9CTufVlnSRg130_assertion
{
miriam-gene:546
a
ncit:C16612
.
lld:C0585216
a
ncit:C7057
.
dgn-gda:DGN69257c0b7ee46e8dea9d70c0dbcbbd32
sio:SIO_000628
miriam-gene:546
,
lld:C0585216
;
a
sio:SIO_001121
.
}
dgn-np:NP928443.RAHUXdUYSbxQCG78kd263sUrop5W4Gpn1k9CTufVlnSRg130_provenance
{
dgn-np:NP928443.RAHUXdUYSbxQCG78kd263sUrop5W4Gpn1k9CTufVlnSRg130_assertion
dcterms:description
"[Acquired mutations in ATRX, a chromatin remodeling gene, have recently been found in 12 patients with typical features of ATMDS, though they have not been detected in MDS patients with similar red blood cell findings but little HbH.]. 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:14576055
;
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:NP928443.RAHUXdUYSbxQCG78kd263sUrop5W4Gpn1k9CTufVlnSRg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:29+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" .
}