@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP687763.RASgvhFzrWZKN0swvfjOZLMvWBDaiH9l1SZ8B7KPMlIGU
> .
@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:NP687763.RASgvhFzrWZKN0swvfjOZLMvWBDaiH9l1SZ8B7KPMlIGU130_head
{
this:
np:hasAssertion
dgn-np:NP687763.RASgvhFzrWZKN0swvfjOZLMvWBDaiH9l1SZ8B7KPMlIGU130_assertion
;
np:hasProvenance
dgn-np:NP687763.RASgvhFzrWZKN0swvfjOZLMvWBDaiH9l1SZ8B7KPMlIGU130_provenance
;
np:hasPublicationInfo
dgn-np:NP687763.RASgvhFzrWZKN0swvfjOZLMvWBDaiH9l1SZ8B7KPMlIGU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP687763.RASgvhFzrWZKN0swvfjOZLMvWBDaiH9l1SZ8B7KPMlIGU130_assertion
a
np:Assertion
.
dgn-np:NP687763.RASgvhFzrWZKN0swvfjOZLMvWBDaiH9l1SZ8B7KPMlIGU130_provenance
a
np:Provenance
.
dgn-np:NP687763.RASgvhFzrWZKN0swvfjOZLMvWBDaiH9l1SZ8B7KPMlIGU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP687763.RASgvhFzrWZKN0swvfjOZLMvWBDaiH9l1SZ8B7KPMlIGU130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0018939
a
ncit:C7057
.
dgn-gda:DGN7f48693dc29ec625ef6a7851be676384
sio:SIO_000628
miriam-gene:7157
,
lld:C0018939
;
a
sio:SIO_001121
.
}
dgn-np:NP687763.RASgvhFzrWZKN0swvfjOZLMvWBDaiH9l1SZ8B7KPMlIGU130_provenance
{
dgn-np:NP687763.RASgvhFzrWZKN0swvfjOZLMvWBDaiH9l1SZ8B7KPMlIGU130_assertion
dcterms:description
"[To assess the utility and efficiency of the PRINS method in the detection of RB1 and p53 deletions, we evaluated 10 patients with hematological disorders and known rearrangements, i.e., deletions involving 13q14 and 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:11807886
;
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:NP687763.RASgvhFzrWZKN0swvfjOZLMvWBDaiH9l1SZ8B7KPMlIGU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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" .
}