@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP482311.RAbiHL2N5r1Qbh-xnCppO3lQgsErdoM537YNvB6KUC0ZE
> .
@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:NP482311.RAbiHL2N5r1Qbh-xnCppO3lQgsErdoM537YNvB6KUC0ZE130_head
{
this:
np:hasAssertion
dgn-np:NP482311.RAbiHL2N5r1Qbh-xnCppO3lQgsErdoM537YNvB6KUC0ZE130_assertion
;
np:hasProvenance
dgn-np:NP482311.RAbiHL2N5r1Qbh-xnCppO3lQgsErdoM537YNvB6KUC0ZE130_provenance
;
np:hasPublicationInfo
dgn-np:NP482311.RAbiHL2N5r1Qbh-xnCppO3lQgsErdoM537YNvB6KUC0ZE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP482311.RAbiHL2N5r1Qbh-xnCppO3lQgsErdoM537YNvB6KUC0ZE130_assertion
a
np:Assertion
.
dgn-np:NP482311.RAbiHL2N5r1Qbh-xnCppO3lQgsErdoM537YNvB6KUC0ZE130_provenance
a
np:Provenance
.
dgn-np:NP482311.RAbiHL2N5r1Qbh-xnCppO3lQgsErdoM537YNvB6KUC0ZE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP482311.RAbiHL2N5r1Qbh-xnCppO3lQgsErdoM537YNvB6KUC0ZE130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0008479
a
ncit:C7057
.
dgn-gda:DGN40e909c1a7472da37cd1c3465a887cad
sio:SIO_000628
miriam-gene:7157
,
lld:C0008479
;
a
sio:SIO_001121
.
}
dgn-np:NP482311.RAbiHL2N5r1Qbh-xnCppO3lQgsErdoM537YNvB6KUC0ZE130_provenance
{
dgn-np:NP482311.RAbiHL2N5r1Qbh-xnCppO3lQgsErdoM537YNvB6KUC0ZE130_assertion
dcterms:description
"[Loss of heterozygosity analysis demonstrated allelic loss at 9p22 and 18q21, but neither in the region of the Rb gene on chromosome 13q nor at the p53 locus on chromosome 17p where allelic loss has already been reported in chondrosarcomas.]. 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:11859213
;
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:NP482311.RAbiHL2N5r1Qbh-xnCppO3lQgsErdoM537YNvB6KUC0ZE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:48+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" .
}