@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP296711.RAhebWRsGfvX7UmJNi7N_q2vQ6EE9ysagTzg9wawZPqMk
> .
@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:NP296711.RAhebWRsGfvX7UmJNi7N_q2vQ6EE9ysagTzg9wawZPqMk130_head
{
this:
np:hasAssertion
dgn-np:NP296711.RAhebWRsGfvX7UmJNi7N_q2vQ6EE9ysagTzg9wawZPqMk130_assertion
;
np:hasProvenance
dgn-np:NP296711.RAhebWRsGfvX7UmJNi7N_q2vQ6EE9ysagTzg9wawZPqMk130_provenance
;
np:hasPublicationInfo
dgn-np:NP296711.RAhebWRsGfvX7UmJNi7N_q2vQ6EE9ysagTzg9wawZPqMk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP296711.RAhebWRsGfvX7UmJNi7N_q2vQ6EE9ysagTzg9wawZPqMk130_assertion
a
np:Assertion
.
dgn-np:NP296711.RAhebWRsGfvX7UmJNi7N_q2vQ6EE9ysagTzg9wawZPqMk130_provenance
a
np:Provenance
.
dgn-np:NP296711.RAhebWRsGfvX7UmJNi7N_q2vQ6EE9ysagTzg9wawZPqMk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP296711.RAhebWRsGfvX7UmJNi7N_q2vQ6EE9ysagTzg9wawZPqMk130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGNd578f53baef78ba3fb3f0afce128c415
sio:SIO_000628
miriam-gene:7248
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP296711.RAhebWRsGfvX7UmJNi7N_q2vQ6EE9ysagTzg9wawZPqMk130_provenance
{
dgn-np:NP296711.RAhebWRsGfvX7UmJNi7N_q2vQ6EE9ysagTzg9wawZPqMk130_assertion
dcterms:description
"[The combination of LCM, MDA and gaCGH is ideally suited for the identification of CNAs from small cell clusters and may assist in the discovery of potential genomic markers for early diagnosis, or identify the location of tumour suppressor genes (TSG) or oncogenes previously unreported in HPIN and CaP.]. 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:16573809
;
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:NP296711.RAhebWRsGfvX7UmJNi7N_q2vQ6EE9ysagTzg9wawZPqMk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}