@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP385113.RARy5W6oVZMfkcBlYFF_XEOyy6IJZAVXdnn8LNoqdafdY
> .
@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:NP385113.RARy5W6oVZMfkcBlYFF_XEOyy6IJZAVXdnn8LNoqdafdY130_head
{
this:
np:hasAssertion
dgn-np:NP385113.RARy5W6oVZMfkcBlYFF_XEOyy6IJZAVXdnn8LNoqdafdY130_assertion
;
np:hasProvenance
dgn-np:NP385113.RARy5W6oVZMfkcBlYFF_XEOyy6IJZAVXdnn8LNoqdafdY130_provenance
;
np:hasPublicationInfo
dgn-np:NP385113.RARy5W6oVZMfkcBlYFF_XEOyy6IJZAVXdnn8LNoqdafdY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP385113.RARy5W6oVZMfkcBlYFF_XEOyy6IJZAVXdnn8LNoqdafdY130_assertion
a
np:Assertion
.
dgn-np:NP385113.RARy5W6oVZMfkcBlYFF_XEOyy6IJZAVXdnn8LNoqdafdY130_provenance
a
np:Provenance
.
dgn-np:NP385113.RARy5W6oVZMfkcBlYFF_XEOyy6IJZAVXdnn8LNoqdafdY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP385113.RARy5W6oVZMfkcBlYFF_XEOyy6IJZAVXdnn8LNoqdafdY130_assertion
{
miriam-gene:207
a
ncit:C16612
.
lld:C0598935
a
ncit:C7057
.
dgn-gda:DGN86b9dde84ed2572938190c71d4520e37
sio:SIO_000628
miriam-gene:207
,
lld:C0598935
;
a
sio:SIO_001121
.
}
dgn-np:NP385113.RARy5W6oVZMfkcBlYFF_XEOyy6IJZAVXdnn8LNoqdafdY130_provenance
{
dgn-np:NP385113.RARy5W6oVZMfkcBlYFF_XEOyy6IJZAVXdnn8LNoqdafdY130_assertion
dcterms:description
"[Tumor initiation required superseding a rate-limiting step between simple and nodular hyperplasia, the latter of which is marked by the emergence of mesenchymal components and the coactivation of AKT and STAT pathways as well as PTEN inactivation.]. 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:17256055
;
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:NP385113.RARy5W6oVZMfkcBlYFF_XEOyy6IJZAVXdnn8LNoqdafdY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:49+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" .
}