@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP404366.RA7hLKN0gPxSyVE4flM40w60xKl7faOMoNtiuXS6HBAPY
> .
@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:NP404366.RA7hLKN0gPxSyVE4flM40w60xKl7faOMoNtiuXS6HBAPY130_head
{
this:
np:hasAssertion
dgn-np:NP404366.RA7hLKN0gPxSyVE4flM40w60xKl7faOMoNtiuXS6HBAPY130_assertion
;
np:hasProvenance
dgn-np:NP404366.RA7hLKN0gPxSyVE4flM40w60xKl7faOMoNtiuXS6HBAPY130_provenance
;
np:hasPublicationInfo
dgn-np:NP404366.RA7hLKN0gPxSyVE4flM40w60xKl7faOMoNtiuXS6HBAPY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP404366.RA7hLKN0gPxSyVE4flM40w60xKl7faOMoNtiuXS6HBAPY130_assertion
a
np:Assertion
.
dgn-np:NP404366.RA7hLKN0gPxSyVE4flM40w60xKl7faOMoNtiuXS6HBAPY130_provenance
a
np:Provenance
.
dgn-np:NP404366.RA7hLKN0gPxSyVE4flM40w60xKl7faOMoNtiuXS6HBAPY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP404366.RA7hLKN0gPxSyVE4flM40w60xKl7faOMoNtiuXS6HBAPY130_assertion
{
miriam-gene:3930
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN39272349b8d8d95531483aaf9dcb2782
sio:SIO_000628
miriam-gene:3930
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP404366.RA7hLKN0gPxSyVE4flM40w60xKl7faOMoNtiuXS6HBAPY130_provenance
{
dgn-np:NP404366.RA7hLKN0gPxSyVE4flM40w60xKl7faOMoNtiuXS6HBAPY130_assertion
dcterms:description
"[By in situ hybridization on chromosome, phytohemagglutinin (PHA)-stimulated lymphocytes obtained from normal individuals showed slight polymorphism in terms of distribution of rDNA among Nucleolar Organizer Region (NOR) chromosomes probably due to racial differences, although their interindividual distinct polymorphism had been reported in the U.S.A. Three chronic and one acute myelogenous leukemias (CML and AML) and one chronic monocytic leukemia (CMoL) were also analysed for the distribution of rDNA among NORs.]. 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:2796260
;
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:NP404366.RA7hLKN0gPxSyVE4flM40w60xKl7faOMoNtiuXS6HBAPY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}