@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP794317.RASXw0qPG5rXwlEBSv0hBS6xwzmr1Udldiof3LjUhek8s
> .
@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:NP794317.RASXw0qPG5rXwlEBSv0hBS6xwzmr1Udldiof3LjUhek8s130_head
{
this:
np:hasAssertion
dgn-np:NP794317.RASXw0qPG5rXwlEBSv0hBS6xwzmr1Udldiof3LjUhek8s130_assertion
;
np:hasProvenance
dgn-np:NP794317.RASXw0qPG5rXwlEBSv0hBS6xwzmr1Udldiof3LjUhek8s130_provenance
;
np:hasPublicationInfo
dgn-np:NP794317.RASXw0qPG5rXwlEBSv0hBS6xwzmr1Udldiof3LjUhek8s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP794317.RASXw0qPG5rXwlEBSv0hBS6xwzmr1Udldiof3LjUhek8s130_assertion
a
np:Assertion
.
dgn-np:NP794317.RASXw0qPG5rXwlEBSv0hBS6xwzmr1Udldiof3LjUhek8s130_provenance
a
np:Provenance
.
dgn-np:NP794317.RASXw0qPG5rXwlEBSv0hBS6xwzmr1Udldiof3LjUhek8s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP794317.RASXw0qPG5rXwlEBSv0hBS6xwzmr1Udldiof3LjUhek8s130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0040028
a
ncit:C7057
.
dgn-gda:DGN6ac4dc1bda5c89015561d36a5b665dc5
sio:SIO_000628
miriam-gene:1437
,
lld:C0040028
;
a
sio:SIO_001121
.
}
dgn-np:NP794317.RASXw0qPG5rXwlEBSv0hBS6xwzmr1Udldiof3LjUhek8s130_provenance
{
dgn-np:NP794317.RASXw0qPG5rXwlEBSv0hBS6xwzmr1Udldiof3LjUhek8s130_assertion
dcterms:description
"[Restriction fragment length polymorphisms (RFLP) of the X-chromosome genes phosphoglycerate kinase and hypoxanthine phosphoribosyl transferase were used in conjunction with cytogenetic analysis to study the clonality of hematopoiesis in four female patients with myelodysplastic syndromes, treated with either granulocyte-macrophage colony-stimulating factor (GM-CSF) or interleukin-3 (IL-3), and in one patient with essential thrombocythemia (ET) treated with IL-3.]. 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:1676079
;
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:NP794317.RASXw0qPG5rXwlEBSv0hBS6xwzmr1Udldiof3LjUhek8s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:08+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" .
}