@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP489998.RAMMYx_jPR0c1C6zWspV701k6-i-Z2el8B_PlrqH-0jXs
> .
@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:NP489998.RAMMYx_jPR0c1C6zWspV701k6-i-Z2el8B_PlrqH-0jXs130_head
{
this:
np:hasAssertion
dgn-np:NP489998.RAMMYx_jPR0c1C6zWspV701k6-i-Z2el8B_PlrqH-0jXs130_assertion
;
np:hasProvenance
dgn-np:NP489998.RAMMYx_jPR0c1C6zWspV701k6-i-Z2el8B_PlrqH-0jXs130_provenance
;
np:hasPublicationInfo
dgn-np:NP489998.RAMMYx_jPR0c1C6zWspV701k6-i-Z2el8B_PlrqH-0jXs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP489998.RAMMYx_jPR0c1C6zWspV701k6-i-Z2el8B_PlrqH-0jXs130_assertion
a
np:Assertion
.
dgn-np:NP489998.RAMMYx_jPR0c1C6zWspV701k6-i-Z2el8B_PlrqH-0jXs130_provenance
a
np:Provenance
.
dgn-np:NP489998.RAMMYx_jPR0c1C6zWspV701k6-i-Z2el8B_PlrqH-0jXs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP489998.RAMMYx_jPR0c1C6zWspV701k6-i-Z2el8B_PlrqH-0jXs130_assertion
{
miriam-gene:5934
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN0eb1bd25ea301c6adfd95bd115e7c09e
sio:SIO_000628
miriam-gene:5934
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP489998.RAMMYx_jPR0c1C6zWspV701k6-i-Z2el8B_PlrqH-0jXs130_provenance
{
dgn-np:NP489998.RAMMYx_jPR0c1C6zWspV701k6-i-Z2el8B_PlrqH-0jXs130_assertion
dcterms:description
"[Deletions of chromosome 16q have been found in several human neoplasias (including breast, ovarian, hepatic, and prostatic cancers) which is in support of an involvement of RB2 in human cancer as a tumor suppressor gene.]. 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:8247552
;
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:NP489998.RAMMYx_jPR0c1C6zWspV701k6-i-Z2el8B_PlrqH-0jXs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:52+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" .
}