@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP272957.RA6bKnBBpxyDeWb0q3dYlP67ol8nCZ7PCKuXJVnG2F_5o
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP272957.RA6bKnBBpxyDeWb0q3dYlP67ol8nCZ7PCKuXJVnG2F_5o130_head
{
this:
np:hasAssertion
dgn-np:NP272957.RA6bKnBBpxyDeWb0q3dYlP67ol8nCZ7PCKuXJVnG2F_5o130_assertion
;
np:hasProvenance
dgn-np:NP272957.RA6bKnBBpxyDeWb0q3dYlP67ol8nCZ7PCKuXJVnG2F_5o130_provenance
;
np:hasPublicationInfo
dgn-np:NP272957.RA6bKnBBpxyDeWb0q3dYlP67ol8nCZ7PCKuXJVnG2F_5o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP272957.RA6bKnBBpxyDeWb0q3dYlP67ol8nCZ7PCKuXJVnG2F_5o130_assertion
a
np:Assertion
.
dgn-np:NP272957.RA6bKnBBpxyDeWb0q3dYlP67ol8nCZ7PCKuXJVnG2F_5o130_provenance
a
np:Provenance
.
dgn-np:NP272957.RA6bKnBBpxyDeWb0q3dYlP67ol8nCZ7PCKuXJVnG2F_5o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP272957.RA6bKnBBpxyDeWb0q3dYlP67ol8nCZ7PCKuXJVnG2F_5o130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0001815
a
ncit:C7057
.
dgn-gda:DGN3a436577ca0bde925dc29604b776aec0
sio:SIO_000628
miriam-gene:675
,
lld:C0001815
;
a
sio:SIO_001121
.
}
dgn-np:NP272957.RA6bKnBBpxyDeWb0q3dYlP67ol8nCZ7PCKuXJVnG2F_5o130_provenance
{
dgn-np:NP272957.RA6bKnBBpxyDeWb0q3dYlP67ol8nCZ7PCKuXJVnG2F_5o130_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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP272957.RA6bKnBBpxyDeWb0q3dYlP67ol8nCZ7PCKuXJVnG2F_5o130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:15+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}