@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP425701.RAJwYhtr1020CFC6r2zoRqdEpzIAGvkNV0OL_1bPzS8IM
> .
@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:NP425701.RAJwYhtr1020CFC6r2zoRqdEpzIAGvkNV0OL_1bPzS8IM130_head
{
this:
np:hasAssertion
dgn-np:NP425701.RAJwYhtr1020CFC6r2zoRqdEpzIAGvkNV0OL_1bPzS8IM130_assertion
;
np:hasProvenance
dgn-np:NP425701.RAJwYhtr1020CFC6r2zoRqdEpzIAGvkNV0OL_1bPzS8IM130_provenance
;
np:hasPublicationInfo
dgn-np:NP425701.RAJwYhtr1020CFC6r2zoRqdEpzIAGvkNV0OL_1bPzS8IM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP425701.RAJwYhtr1020CFC6r2zoRqdEpzIAGvkNV0OL_1bPzS8IM130_assertion
a
np:Assertion
.
dgn-np:NP425701.RAJwYhtr1020CFC6r2zoRqdEpzIAGvkNV0OL_1bPzS8IM130_provenance
a
np:Provenance
.
dgn-np:NP425701.RAJwYhtr1020CFC6r2zoRqdEpzIAGvkNV0OL_1bPzS8IM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP425701.RAJwYhtr1020CFC6r2zoRqdEpzIAGvkNV0OL_1bPzS8IM130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0267244
a
ncit:C7057
.
dgn-gda:DGNd768ff15f26cc8c6a1df9885f5766c71
sio:SIO_000628
miriam-gene:675
,
lld:C0267244
;
a
sio:SIO_001121
.
}
dgn-np:NP425701.RAJwYhtr1020CFC6r2zoRqdEpzIAGvkNV0OL_1bPzS8IM130_provenance
{
dgn-np:NP425701.RAJwYhtr1020CFC6r2zoRqdEpzIAGvkNV0OL_1bPzS8IM130_assertion
dcterms:description
"[Representational difference analysis (RDA) uses selective hybridization and the polymerase chain reaction (PCR) to isolate regions of chromosomal loss and has facilitated the identification of tumor suppressor genes, such as BRCA2 and PTEN.]. 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:10379873
;
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:NP425701.RAJwYhtr1020CFC6r2zoRqdEpzIAGvkNV0OL_1bPzS8IM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:12+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" .
}