@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP833606.RAni35wGhyJuXcQUbJvHbl1asaIbLbXkk_W9mW9ybLOXs
> .
@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:NP833606.RAni35wGhyJuXcQUbJvHbl1asaIbLbXkk_W9mW9ybLOXs130_head
{
this:
np:hasAssertion
dgn-np:NP833606.RAni35wGhyJuXcQUbJvHbl1asaIbLbXkk_W9mW9ybLOXs130_assertion
;
np:hasProvenance
dgn-np:NP833606.RAni35wGhyJuXcQUbJvHbl1asaIbLbXkk_W9mW9ybLOXs130_provenance
;
np:hasPublicationInfo
dgn-np:NP833606.RAni35wGhyJuXcQUbJvHbl1asaIbLbXkk_W9mW9ybLOXs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP833606.RAni35wGhyJuXcQUbJvHbl1asaIbLbXkk_W9mW9ybLOXs130_assertion
a
np:Assertion
.
dgn-np:NP833606.RAni35wGhyJuXcQUbJvHbl1asaIbLbXkk_W9mW9ybLOXs130_provenance
a
np:Provenance
.
dgn-np:NP833606.RAni35wGhyJuXcQUbJvHbl1asaIbLbXkk_W9mW9ybLOXs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP833606.RAni35wGhyJuXcQUbJvHbl1asaIbLbXkk_W9mW9ybLOXs130_assertion
{
miriam-gene:2048
a
ncit:C16612
.
lld:C0007102
a
ncit:C7057
.
dgn-gda:DGNc7306268421539fe489f3043a1fd572d
sio:SIO_000628
miriam-gene:2048
,
lld:C0007102
;
a
sio:SIO_001121
.
}
dgn-np:NP833606.RAni35wGhyJuXcQUbJvHbl1asaIbLbXkk_W9mW9ybLOXs130_provenance
{
dgn-np:NP833606.RAni35wGhyJuXcQUbJvHbl1asaIbLbXkk_W9mW9ybLOXs130_assertion
dcterms:description
"[So, despite its overexpression in some kind of tumors, we decided to study the possibility of involvement in the EphB2 gene (EPHB2) mutation in colon cancers, because some of the well known tumor suppressor genes (e.g.]. 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:11166921
;
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:NP833606.RAni35wGhyJuXcQUbJvHbl1asaIbLbXkk_W9mW9ybLOXs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:30+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" .
}