@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP553563.RAFjQXw_jlE2eNDOPJmyJ0u_1bnPFA1Tg11L3MwKHzU0w
> .
@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:NP553563.RAFjQXw_jlE2eNDOPJmyJ0u_1bnPFA1Tg11L3MwKHzU0w130_head
{
this:
np:hasAssertion
dgn-np:NP553563.RAFjQXw_jlE2eNDOPJmyJ0u_1bnPFA1Tg11L3MwKHzU0w130_assertion
;
np:hasProvenance
dgn-np:NP553563.RAFjQXw_jlE2eNDOPJmyJ0u_1bnPFA1Tg11L3MwKHzU0w130_provenance
;
np:hasPublicationInfo
dgn-np:NP553563.RAFjQXw_jlE2eNDOPJmyJ0u_1bnPFA1Tg11L3MwKHzU0w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP553563.RAFjQXw_jlE2eNDOPJmyJ0u_1bnPFA1Tg11L3MwKHzU0w130_assertion
a
np:Assertion
.
dgn-np:NP553563.RAFjQXw_jlE2eNDOPJmyJ0u_1bnPFA1Tg11L3MwKHzU0w130_provenance
a
np:Provenance
.
dgn-np:NP553563.RAFjQXw_jlE2eNDOPJmyJ0u_1bnPFA1Tg11L3MwKHzU0w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP553563.RAFjQXw_jlE2eNDOPJmyJ0u_1bnPFA1Tg11L3MwKHzU0w130_assertion
{
miriam-gene:5367
a
ncit:C16612
.
lld:C0002871
a
ncit:C7057
.
dgn-gda:DGN13391311a916ff5d6caaad3caae9f6e2
sio:SIO_000628
miriam-gene:5367
,
lld:C0002871
;
a
sio:SIO_001121
.
}
dgn-np:NP553563.RAFjQXw_jlE2eNDOPJmyJ0u_1bnPFA1Tg11L3MwKHzU0w130_provenance
{
dgn-np:NP553563.RAFjQXw_jlE2eNDOPJmyJ0u_1bnPFA1Tg11L3MwKHzU0w130_assertion
dcterms:description
"[Patients with low hemoglobin (Hb), low mean cell volume (MCV) and mean cell hemoglobin (MCH) including anemia, microcytosis, hypochromic hemolysis and target cells, were refered for the identification of hemoglobinopathy by molecular methods.]. 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:12757239
;
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:NP553563.RAFjQXw_jlE2eNDOPJmyJ0u_1bnPFA1Tg11L3MwKHzU0w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:33+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" .
}