@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP405577.RAve0TXVSMwaNVRNTUFgCu8PfDH1EYgqgM64WmmMsZf2o
> .
@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:NP405577.RAve0TXVSMwaNVRNTUFgCu8PfDH1EYgqgM64WmmMsZf2o130_head
{
this:
np:hasAssertion
dgn-np:NP405577.RAve0TXVSMwaNVRNTUFgCu8PfDH1EYgqgM64WmmMsZf2o130_assertion
;
np:hasProvenance
dgn-np:NP405577.RAve0TXVSMwaNVRNTUFgCu8PfDH1EYgqgM64WmmMsZf2o130_provenance
;
np:hasPublicationInfo
dgn-np:NP405577.RAve0TXVSMwaNVRNTUFgCu8PfDH1EYgqgM64WmmMsZf2o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP405577.RAve0TXVSMwaNVRNTUFgCu8PfDH1EYgqgM64WmmMsZf2o130_assertion
a
np:Assertion
.
dgn-np:NP405577.RAve0TXVSMwaNVRNTUFgCu8PfDH1EYgqgM64WmmMsZf2o130_provenance
a
np:Provenance
.
dgn-np:NP405577.RAve0TXVSMwaNVRNTUFgCu8PfDH1EYgqgM64WmmMsZf2o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP405577.RAve0TXVSMwaNVRNTUFgCu8PfDH1EYgqgM64WmmMsZf2o130_assertion
{
miriam-gene:429
a
ncit:C16612
.
lld:C0027819
a
ncit:C7057
.
dgn-gda:DGN9d933929775be9709166377b248a9a79
sio:SIO_000628
miriam-gene:429
,
lld:C0027819
;
a
sio:SIO_001121
.
}
dgn-np:NP405577.RAve0TXVSMwaNVRNTUFgCu8PfDH1EYgqgM64WmmMsZf2o130_provenance
{
dgn-np:NP405577.RAve0TXVSMwaNVRNTUFgCu8PfDH1EYgqgM64WmmMsZf2o130_assertion
dcterms:description
"[To investigate the functional significance of human MASH1 (hASH1) in the pathogenesis of neuroblastoma, which is originated from autonomic precursor cells, we studied hASH1 gene expression in primary neuroblastomas and human nueroblastoma cell lines.]. 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:11464865
;
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:NP405577.RAve0TXVSMwaNVRNTUFgCu8PfDH1EYgqgM64WmmMsZf2o130_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" .
}