@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw
> .
@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:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_head
{
this:
np:hasAssertion
dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_assertion
;
np:hasProvenance
dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_provenance
;
np:hasPublicationInfo
dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_assertion
a
np:Assertion
.
dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_provenance
a
np:Provenance
.
dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_assertion
{
miriam-gene:6927
a
ncit:C16612
.
lld:C0541760
a
ncit:C7057
.
dgn-gda:DGN25a10b10b43643f9c93af9adbedc9186
sio:SIO_000628
miriam-gene:6927
,
lld:C0541760
;
a
sio:SIO_001121
.
}
dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_provenance
{
dgn-np:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_assertion
dcterms:description
"[These 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: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:NP425140.RACWBHGLOcqQ1Cb777Bo5MjdjrgiSiv85rIjTc9csBkAw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:12+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" .
}