@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP582257.RATZM2VHXKPXgpdGk72LXUX5Hy6LHXvrQDYLn9EL07uBY
> .
@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:NP582257.RATZM2VHXKPXgpdGk72LXUX5Hy6LHXvrQDYLn9EL07uBY130_head
{
this:
np:hasAssertion
dgn-np:NP582257.RATZM2VHXKPXgpdGk72LXUX5Hy6LHXvrQDYLn9EL07uBY130_assertion
;
np:hasProvenance
dgn-np:NP582257.RATZM2VHXKPXgpdGk72LXUX5Hy6LHXvrQDYLn9EL07uBY130_provenance
;
np:hasPublicationInfo
dgn-np:NP582257.RATZM2VHXKPXgpdGk72LXUX5Hy6LHXvrQDYLn9EL07uBY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP582257.RATZM2VHXKPXgpdGk72LXUX5Hy6LHXvrQDYLn9EL07uBY130_assertion
a
np:Assertion
.
dgn-np:NP582257.RATZM2VHXKPXgpdGk72LXUX5Hy6LHXvrQDYLn9EL07uBY130_provenance
a
np:Provenance
.
dgn-np:NP582257.RATZM2VHXKPXgpdGk72LXUX5Hy6LHXvrQDYLn9EL07uBY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP582257.RATZM2VHXKPXgpdGk72LXUX5Hy6LHXvrQDYLn9EL07uBY130_assertion
{
miriam-gene:84668
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN245dfb23b849fdfb1bbde1820f3ccf24
sio:SIO_000628
miriam-gene:84668
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP582257.RATZM2VHXKPXgpdGk72LXUX5Hy6LHXvrQDYLn9EL07uBY130_provenance
{
dgn-np:NP582257.RATZM2VHXKPXgpdGk72LXUX5Hy6LHXvrQDYLn9EL07uBY130_assertion
dcterms:description
"[This in vitro data on the incidence of IVT in clinically affected members from HCC families suggested that this putative biomarker for colon cancer proneness may ultimately be useful in identification of such increased genetic risk for colon cancer in such HCC families and further supported the hypothesis that germinal mutations for cancer proneness (detected by in vitro expression of IVT) are relevant in the development of HCC.]. 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:3168398
;
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:NP582257.RATZM2VHXKPXgpdGk72LXUX5Hy6LHXvrQDYLn9EL07uBY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:50+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
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dgn-void:disgenetrdf
pav:version
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}