@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP584013.RAFIvYhJfOGk4or6BR2fz6NMNZVtwRyOZuHOyGeuPf8Dg
> .
@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:NP584013.RAFIvYhJfOGk4or6BR2fz6NMNZVtwRyOZuHOyGeuPf8Dg130_head
{
this:
np:hasAssertion
dgn-np:NP584013.RAFIvYhJfOGk4or6BR2fz6NMNZVtwRyOZuHOyGeuPf8Dg130_assertion
;
np:hasProvenance
dgn-np:NP584013.RAFIvYhJfOGk4or6BR2fz6NMNZVtwRyOZuHOyGeuPf8Dg130_provenance
;
np:hasPublicationInfo
dgn-np:NP584013.RAFIvYhJfOGk4or6BR2fz6NMNZVtwRyOZuHOyGeuPf8Dg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP584013.RAFIvYhJfOGk4or6BR2fz6NMNZVtwRyOZuHOyGeuPf8Dg130_assertion
a
np:Assertion
.
dgn-np:NP584013.RAFIvYhJfOGk4or6BR2fz6NMNZVtwRyOZuHOyGeuPf8Dg130_provenance
a
np:Provenance
.
dgn-np:NP584013.RAFIvYhJfOGk4or6BR2fz6NMNZVtwRyOZuHOyGeuPf8Dg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP584013.RAFIvYhJfOGk4or6BR2fz6NMNZVtwRyOZuHOyGeuPf8Dg130_assertion
{
miriam-gene:3048
a
ncit:C16612
.
lld:C0271979
a
ncit:C7057
.
dgn-gda:DGNc5af413a9cc49e4ab1a19610093ff078
sio:SIO_000628
miriam-gene:3048
,
lld:C0271979
;
a
sio:SIO_001121
.
}
dgn-np:NP584013.RAFIvYhJfOGk4or6BR2fz6NMNZVtwRyOZuHOyGeuPf8Dg130_provenance
{
dgn-np:NP584013.RAFIvYhJfOGk4or6BR2fz6NMNZVtwRyOZuHOyGeuPf8Dg130_assertion
dcterms:description
"[This report describes four unrelated Greek patients (one child and three adults) who all had an atypical thalassemia intermedia phenotype, characterized by chronic moderate anemia with mild hemolysis in some cases, and the absence of abnormal hemoglobin (Hb) fractions.]. 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:18654887
;
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:NP584013.RAFIvYhJfOGk4or6BR2fz6NMNZVtwRyOZuHOyGeuPf8Dg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:51+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" .
}