@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP132410.RAVXS6fLkdMgTMKCt2Xl-VwOXxnkdZTKG6576si5Er3WA
> .
@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:NP132410.RAVXS6fLkdMgTMKCt2Xl-VwOXxnkdZTKG6576si5Er3WA130_head
{
this:
np:hasAssertion
dgn-np:NP132410.RAVXS6fLkdMgTMKCt2Xl-VwOXxnkdZTKG6576si5Er3WA130_assertion
;
np:hasProvenance
dgn-np:NP132410.RAVXS6fLkdMgTMKCt2Xl-VwOXxnkdZTKG6576si5Er3WA130_provenance
;
np:hasPublicationInfo
dgn-np:NP132410.RAVXS6fLkdMgTMKCt2Xl-VwOXxnkdZTKG6576si5Er3WA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP132410.RAVXS6fLkdMgTMKCt2Xl-VwOXxnkdZTKG6576si5Er3WA130_assertion
a
np:Assertion
.
dgn-np:NP132410.RAVXS6fLkdMgTMKCt2Xl-VwOXxnkdZTKG6576si5Er3WA130_provenance
a
np:Provenance
.
dgn-np:NP132410.RAVXS6fLkdMgTMKCt2Xl-VwOXxnkdZTKG6576si5Er3WA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP132410.RAVXS6fLkdMgTMKCt2Xl-VwOXxnkdZTKG6576si5Er3WA130_assertion
{
miriam-gene:6927
a
ncit:C16612
.
lld:C0001430
a
ncit:C7057
.
dgn-gda:DGN495b0697f2761bd59a8f4318bbabc00b
sio:SIO_000628
miriam-gene:6927
,
lld:C0001430
;
a
sio:SIO_001123
.
}
dgn-np:NP132410.RAVXS6fLkdMgTMKCt2Xl-VwOXxnkdZTKG6576si5Er3WA130_provenance
{
dgn-np:NP132410.RAVXS6fLkdMgTMKCt2Xl-VwOXxnkdZTKG6576si5Er3WA130_assertion
dcterms:description
"[results indicate that inactivation of TCF1, whether sporadic or associated with MODY3, is an important genetic event in the occurrence of human liver adenoma, and may be an early step in the development of some HCCs ]. 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:12355088
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP132410.RAVXS6fLkdMgTMKCt2Xl-VwOXxnkdZTKG6576si5Er3WA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:09+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" .
}