@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP880653.RA2TUxlB7In9nuBPaeJ7Ki33999zbSvuzGYjUylvFQlE4
> .
@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:NP880653.RA2TUxlB7In9nuBPaeJ7Ki33999zbSvuzGYjUylvFQlE4130_head
{
this:
np:hasAssertion
dgn-np:NP880653.RA2TUxlB7In9nuBPaeJ7Ki33999zbSvuzGYjUylvFQlE4130_assertion
;
np:hasProvenance
dgn-np:NP880653.RA2TUxlB7In9nuBPaeJ7Ki33999zbSvuzGYjUylvFQlE4130_provenance
;
np:hasPublicationInfo
dgn-np:NP880653.RA2TUxlB7In9nuBPaeJ7Ki33999zbSvuzGYjUylvFQlE4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP880653.RA2TUxlB7In9nuBPaeJ7Ki33999zbSvuzGYjUylvFQlE4130_assertion
a
np:Assertion
.
dgn-np:NP880653.RA2TUxlB7In9nuBPaeJ7Ki33999zbSvuzGYjUylvFQlE4130_provenance
a
np:Provenance
.
dgn-np:NP880653.RA2TUxlB7In9nuBPaeJ7Ki33999zbSvuzGYjUylvFQlE4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP880653.RA2TUxlB7In9nuBPaeJ7Ki33999zbSvuzGYjUylvFQlE4130_assertion
{
miriam-gene:5925
a
ncit:C16612
.
lld:C0001815
a
ncit:C7057
.
dgn-gda:DGN867cef4a22e6a3b65556f3e4560af994
sio:SIO_000628
miriam-gene:5925
,
lld:C0001815
;
a
sio:SIO_001121
.
}
dgn-np:NP880653.RA2TUxlB7In9nuBPaeJ7Ki33999zbSvuzGYjUylvFQlE4130_provenance
{
dgn-np:NP880653.RA2TUxlB7In9nuBPaeJ7Ki33999zbSvuzGYjUylvFQlE4130_assertion
dcterms:description
"[To identify a commonly deleted region of 13q14 in idiopathic myelofibrosis (IMF), we used fluorescence in situ hybridization analysis to test for deletion of the RB1 and BRCA2 genes, and the microsatellite loci D13S319 and D13S25, in a series of 25 patients.]. 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:11380400
;
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:NP880653.RA2TUxlB7In9nuBPaeJ7Ki33999zbSvuzGYjUylvFQlE4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:58+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" .
}