@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP846984.RABnTv0fVz011z0jY4GOvC1X-u7B_qi_eopIbJxcUqv2M
> .
@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:NP846984.RABnTv0fVz011z0jY4GOvC1X-u7B_qi_eopIbJxcUqv2M130_head
{
this:
np:hasAssertion
dgn-np:NP846984.RABnTv0fVz011z0jY4GOvC1X-u7B_qi_eopIbJxcUqv2M130_assertion
;
np:hasProvenance
dgn-np:NP846984.RABnTv0fVz011z0jY4GOvC1X-u7B_qi_eopIbJxcUqv2M130_provenance
;
np:hasPublicationInfo
dgn-np:NP846984.RABnTv0fVz011z0jY4GOvC1X-u7B_qi_eopIbJxcUqv2M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP846984.RABnTv0fVz011z0jY4GOvC1X-u7B_qi_eopIbJxcUqv2M130_assertion
a
np:Assertion
.
dgn-np:NP846984.RABnTv0fVz011z0jY4GOvC1X-u7B_qi_eopIbJxcUqv2M130_provenance
a
np:Provenance
.
dgn-np:NP846984.RABnTv0fVz011z0jY4GOvC1X-u7B_qi_eopIbJxcUqv2M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP846984.RABnTv0fVz011z0jY4GOvC1X-u7B_qi_eopIbJxcUqv2M130_assertion
{
miriam-gene:6817
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN7313c505b39ff0e8072122d943701806
sio:SIO_000628
miriam-gene:6817
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP846984.RABnTv0fVz011z0jY4GOvC1X-u7B_qi_eopIbJxcUqv2M130_provenance
{
dgn-np:NP846984.RABnTv0fVz011z0jY4GOvC1X-u7B_qi_eopIbJxcUqv2M130_assertion
dcterms:description
"[FVB multiple intestinal neoplasia (Min) mice, which spontaneously develop tumors and flat aberrant crypt foci (ACF) in intestine, were crossed with transgenic FVB mice expressing human SULT1A1 and 1A2 (hSULT) in several tissues, giving rise to wild-type and Min mice with and without hSULT.]. 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:22006426
;
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:NP846984.RABnTv0fVz011z0jY4GOvC1X-u7B_qi_eopIbJxcUqv2M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:38+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" .
}