@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP329522.RA_HweHAWdMHerhVMxb1L16_0l5l2EbsxDJ6UMgu9q64M
> .
@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:NP329522.RA_HweHAWdMHerhVMxb1L16_0l5l2EbsxDJ6UMgu9q64M130_head
{
this:
np:hasAssertion
dgn-np:NP329522.RA_HweHAWdMHerhVMxb1L16_0l5l2EbsxDJ6UMgu9q64M130_assertion
;
np:hasProvenance
dgn-np:NP329522.RA_HweHAWdMHerhVMxb1L16_0l5l2EbsxDJ6UMgu9q64M130_provenance
;
np:hasPublicationInfo
dgn-np:NP329522.RA_HweHAWdMHerhVMxb1L16_0l5l2EbsxDJ6UMgu9q64M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP329522.RA_HweHAWdMHerhVMxb1L16_0l5l2EbsxDJ6UMgu9q64M130_assertion
a
np:Assertion
.
dgn-np:NP329522.RA_HweHAWdMHerhVMxb1L16_0l5l2EbsxDJ6UMgu9q64M130_provenance
a
np:Provenance
.
dgn-np:NP329522.RA_HweHAWdMHerhVMxb1L16_0l5l2EbsxDJ6UMgu9q64M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP329522.RA_HweHAWdMHerhVMxb1L16_0l5l2EbsxDJ6UMgu9q64M130_assertion
{
miriam-gene:7048
a
ncit:C16612
.
lld:C0007102
a
ncit:C7057
.
dgn-gda:DGN8b93ca324cde8fe889b55d776ee0d38e
sio:SIO_000628
miriam-gene:7048
,
lld:C0007102
;
a
sio:SIO_001121
.
}
dgn-np:NP329522.RA_HweHAWdMHerhVMxb1L16_0l5l2EbsxDJ6UMgu9q64M130_provenance
{
dgn-np:NP329522.RA_HweHAWdMHerhVMxb1L16_0l5l2EbsxDJ6UMgu9q64M130_assertion
dcterms:description
"[Through the use of defined cell line systems, we show that both genomic instability and clonal selection of TGFB resistant cells contribute to the high frequency of TGFBR2 mutations in MSI colon cancer.]. 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:17985359
;
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:NP329522.RA_HweHAWdMHerhVMxb1L16_0l5l2EbsxDJ6UMgu9q64M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:14+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" .
}