@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP635493.RAvsBhKxu2FEVUP1tM0fPj3jzkmIw8POiYub2Ng7HhFxE
> .
@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:NP635493.RAvsBhKxu2FEVUP1tM0fPj3jzkmIw8POiYub2Ng7HhFxE130_head
{
this:
np:hasAssertion
dgn-np:NP635493.RAvsBhKxu2FEVUP1tM0fPj3jzkmIw8POiYub2Ng7HhFxE130_assertion
;
np:hasProvenance
dgn-np:NP635493.RAvsBhKxu2FEVUP1tM0fPj3jzkmIw8POiYub2Ng7HhFxE130_provenance
;
np:hasPublicationInfo
dgn-np:NP635493.RAvsBhKxu2FEVUP1tM0fPj3jzkmIw8POiYub2Ng7HhFxE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP635493.RAvsBhKxu2FEVUP1tM0fPj3jzkmIw8POiYub2Ng7HhFxE130_assertion
a
np:Assertion
.
dgn-np:NP635493.RAvsBhKxu2FEVUP1tM0fPj3jzkmIw8POiYub2Ng7HhFxE130_provenance
a
np:Provenance
.
dgn-np:NP635493.RAvsBhKxu2FEVUP1tM0fPj3jzkmIw8POiYub2Ng7HhFxE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP635493.RAvsBhKxu2FEVUP1tM0fPj3jzkmIw8POiYub2Ng7HhFxE130_assertion
{
miriam-gene:5925
a
ncit:C16612
.
lld:C0280100
a
ncit:C7057
.
dgn-gda:DGNa698383bc0c670da4f68ca330436a805
sio:SIO_000628
miriam-gene:5925
,
lld:C0280100
;
a
sio:SIO_001121
.
}
dgn-np:NP635493.RAvsBhKxu2FEVUP1tM0fPj3jzkmIw8POiYub2Ng7HhFxE130_provenance
{
dgn-np:NP635493.RAvsBhKxu2FEVUP1tM0fPj3jzkmIw8POiYub2Ng7HhFxE130_assertion
dcterms:description
"[Studies of mutant genotypes of the retinoblastoma susceptibility gene (RB1) in different solid tumors have mainly been concentrated on the demonstration of loss of heterozygosity (LOH) at both internal and external polymorphic sites.]. 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:1381957
;
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:NP635493.RAvsBhKxu2FEVUP1tM0fPj3jzkmIw8POiYub2Ng7HhFxE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:23+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" .
}