@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP440031.RAXTQs5xmwQQngVMZdFtGOQqY7iMHLvEIslw9kN7-nFRc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP440031.RAXTQs5xmwQQngVMZdFtGOQqY7iMHLvEIslw9kN7-nFRc130_head
{
this:
np:hasAssertion
dgn-np:NP440031.RAXTQs5xmwQQngVMZdFtGOQqY7iMHLvEIslw9kN7-nFRc130_assertion
;
np:hasProvenance
dgn-np:NP440031.RAXTQs5xmwQQngVMZdFtGOQqY7iMHLvEIslw9kN7-nFRc130_provenance
;
np:hasPublicationInfo
dgn-np:NP440031.RAXTQs5xmwQQngVMZdFtGOQqY7iMHLvEIslw9kN7-nFRc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP440031.RAXTQs5xmwQQngVMZdFtGOQqY7iMHLvEIslw9kN7-nFRc130_assertion
a
np:Assertion
.
dgn-np:NP440031.RAXTQs5xmwQQngVMZdFtGOQqY7iMHLvEIslw9kN7-nFRc130_provenance
a
np:Provenance
.
dgn-np:NP440031.RAXTQs5xmwQQngVMZdFtGOQqY7iMHLvEIslw9kN7-nFRc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP440031.RAXTQs5xmwQQngVMZdFtGOQqY7iMHLvEIslw9kN7-nFRc130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGN0125daefcf8e788f3d12b7057b4b2284
sio:SIO_000628
miriam-gene:7157
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP440031.RAXTQs5xmwQQngVMZdFtGOQqY7iMHLvEIslw9kN7-nFRc130_provenance
{
dgn-np:NP440031.RAXTQs5xmwQQngVMZdFtGOQqY7iMHLvEIslw9kN7-nFRc130_assertion
dcterms:description
"[Although some genetic alterations involving the p53 family, Rb family, and Wnt pathways are particularly important in the development of HCCs, the molecular pathogenesis of HCC differs with etiology in some extent.]. 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:15085488
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP440031.RAXTQs5xmwQQngVMZdFtGOQqY7iMHLvEIslw9kN7-nFRc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:04+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}