@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP405467.RAJv4sRrtVuSTn1kwJb8ULRAOAOiN5WqGqUCXEqyWeM_s
> .
@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:NP405467.RAJv4sRrtVuSTn1kwJb8ULRAOAOiN5WqGqUCXEqyWeM_s130_head
{
this:
np:hasAssertion
dgn-np:NP405467.RAJv4sRrtVuSTn1kwJb8ULRAOAOiN5WqGqUCXEqyWeM_s130_assertion
;
np:hasProvenance
dgn-np:NP405467.RAJv4sRrtVuSTn1kwJb8ULRAOAOiN5WqGqUCXEqyWeM_s130_provenance
;
np:hasPublicationInfo
dgn-np:NP405467.RAJv4sRrtVuSTn1kwJb8ULRAOAOiN5WqGqUCXEqyWeM_s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP405467.RAJv4sRrtVuSTn1kwJb8ULRAOAOiN5WqGqUCXEqyWeM_s130_assertion
a
np:Assertion
.
dgn-np:NP405467.RAJv4sRrtVuSTn1kwJb8ULRAOAOiN5WqGqUCXEqyWeM_s130_provenance
a
np:Provenance
.
dgn-np:NP405467.RAJv4sRrtVuSTn1kwJb8ULRAOAOiN5WqGqUCXEqyWeM_s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP405467.RAJv4sRrtVuSTn1kwJb8ULRAOAOiN5WqGqUCXEqyWeM_s130_assertion
{
miriam-gene:23261
a
ncit:C16612
.
lld:C0700095
a
ncit:C7057
.
dgn-gda:DGNf24c0c50666391553c27e2ab2d7f57d6
sio:SIO_000628
miriam-gene:23261
,
lld:C0700095
;
a
sio:SIO_001121
.
}
dgn-np:NP405467.RAJv4sRrtVuSTn1kwJb8ULRAOAOiN5WqGqUCXEqyWeM_s130_provenance
{
dgn-np:NP405467.RAJv4sRrtVuSTn1kwJb8ULRAOAOiN5WqGqUCXEqyWeM_s130_assertion
dcterms:description
"[Our data suggest that assessment of CAMTA1 expression may improve the prognostic models for neuroblastoma and that it will be important to define the biological function of CAMTA1 in this disease.]. 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:16397034
;
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:NP405467.RAJv4sRrtVuSTn1kwJb8ULRAOAOiN5WqGqUCXEqyWeM_s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:01+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" .
}