@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP622071.RANR6l17rxg4T2kB93lPE6JfB2HEfq86vn7S_Irm-NIDg
> .
@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:NP622071.RANR6l17rxg4T2kB93lPE6JfB2HEfq86vn7S_Irm-NIDg130_head
{
this:
np:hasAssertion
dgn-np:NP622071.RANR6l17rxg4T2kB93lPE6JfB2HEfq86vn7S_Irm-NIDg130_assertion
;
np:hasProvenance
dgn-np:NP622071.RANR6l17rxg4T2kB93lPE6JfB2HEfq86vn7S_Irm-NIDg130_provenance
;
np:hasPublicationInfo
dgn-np:NP622071.RANR6l17rxg4T2kB93lPE6JfB2HEfq86vn7S_Irm-NIDg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP622071.RANR6l17rxg4T2kB93lPE6JfB2HEfq86vn7S_Irm-NIDg130_assertion
a
np:Assertion
.
dgn-np:NP622071.RANR6l17rxg4T2kB93lPE6JfB2HEfq86vn7S_Irm-NIDg130_provenance
a
np:Provenance
.
dgn-np:NP622071.RANR6l17rxg4T2kB93lPE6JfB2HEfq86vn7S_Irm-NIDg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP622071.RANR6l17rxg4T2kB93lPE6JfB2HEfq86vn7S_Irm-NIDg130_assertion
{
miriam-gene:5925
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGNaedb07d0ebb63ccf38f76f0fb6d60e62
sio:SIO_000628
miriam-gene:5925
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP622071.RANR6l17rxg4T2kB93lPE6JfB2HEfq86vn7S_Irm-NIDg130_provenance
{
dgn-np:NP622071.RANR6l17rxg4T2kB93lPE6JfB2HEfq86vn7S_Irm-NIDg130_assertion
dcterms:description
"[Our group modified the primed in situ labeling (PRINS) method to study RB1 and p53 in cultured bone marrow cells from leukemia patients with known deletions within the 13q14 or 17p13 regions.]. 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:16861756
;
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:NP622071.RANR6l17rxg4T2kB93lPE6JfB2HEfq86vn7S_Irm-NIDg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:15+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: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" .
}