@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP298176.RAt6_DiSR5aKkmlvmxa23I-9UZvju_F927zc9dagZr5kQ
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP298176.RAt6_DiSR5aKkmlvmxa23I-9UZvju_F927zc9dagZr5kQ130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP298176.RAt6_DiSR5aKkmlvmxa23I-9UZvju_F927zc9dagZr5kQ130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP298176.RAt6_DiSR5aKkmlvmxa23I-9UZvju_F927zc9dagZr5kQ130_assertion
a
np:Assertion
.
dgn-np:NP298176.RAt6_DiSR5aKkmlvmxa23I-9UZvju_F927zc9dagZr5kQ130_provenance
a
np:Provenance
.
dgn-np:NP298176.RAt6_DiSR5aKkmlvmxa23I-9UZvju_F927zc9dagZr5kQ130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:7157
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN95ea40e35a15c601f266c4c184e6bd76
sio:SIO_000628
miriam-gene:7157
,
lld:C0006142
;
a
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.
}
dgn-np:NP298176.RAt6_DiSR5aKkmlvmxa23I-9UZvju_F927zc9dagZr5kQ130_provenance
{
dgn-np:NP298176.RAt6_DiSR5aKkmlvmxa23I-9UZvju_F927zc9dagZr5kQ130_assertion
dcterms:description
"[We show by laser-assisted microdissection that frequent genetic alterations in non-hereditary invasive human colon and breast cancers (loss of heterozygosity and TP53 mutations) occur not only in the neoplastic epithelial cells, but also in the adjacent fibroblastic tumor stroma and that both components can share clonal features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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miriam-pubmed:11043390
;
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;
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 .
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dgn-np:NP298176.RAt6_DiSR5aKkmlvmxa23I-9UZvju_F927zc9dagZr5kQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:01+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
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<
http://orcid.org/0000-0003-0169-8159
> ;
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"v4.0.0" .
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