@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP798110.RAm7wSk4LKMEOawoXdvhaLX0Vwxt37AiPW5lOFxgWKsbc
> .
@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:NP798110.RAm7wSk4LKMEOawoXdvhaLX0Vwxt37AiPW5lOFxgWKsbc130_head
{
this:
np:hasAssertion
dgn-np:NP798110.RAm7wSk4LKMEOawoXdvhaLX0Vwxt37AiPW5lOFxgWKsbc130_assertion
;
np:hasProvenance
dgn-np:NP798110.RAm7wSk4LKMEOawoXdvhaLX0Vwxt37AiPW5lOFxgWKsbc130_provenance
;
np:hasPublicationInfo
dgn-np:NP798110.RAm7wSk4LKMEOawoXdvhaLX0Vwxt37AiPW5lOFxgWKsbc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP798110.RAm7wSk4LKMEOawoXdvhaLX0Vwxt37AiPW5lOFxgWKsbc130_assertion
a
np:Assertion
.
dgn-np:NP798110.RAm7wSk4LKMEOawoXdvhaLX0Vwxt37AiPW5lOFxgWKsbc130_provenance
a
np:Provenance
.
dgn-np:NP798110.RAm7wSk4LKMEOawoXdvhaLX0Vwxt37AiPW5lOFxgWKsbc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP798110.RAm7wSk4LKMEOawoXdvhaLX0Vwxt37AiPW5lOFxgWKsbc130_assertion
{
miriam-gene:4087
a
ncit:C16612
.
lld:C0235974
a
ncit:C7057
.
dgn-gda:DGN0bdfa6967eb3297e655921ee9a05103b
sio:SIO_000628
miriam-gene:4087
,
lld:C0235974
;
a
sio:SIO_001121
.
}
dgn-np:NP798110.RAm7wSk4LKMEOawoXdvhaLX0Vwxt37AiPW5lOFxgWKsbc130_provenance
{
dgn-np:NP798110.RAm7wSk4LKMEOawoXdvhaLX0Vwxt37AiPW5lOFxgWKsbc130_assertion
dcterms:description
"[Losses of 15q and 18q material are frequent in pancreatic carcinomas, and in order to map the extent of 15q and 18q deletions and to investigate further the involvement of SMAD4 and the possible function of SMAD2 and SMAD3 as tumor suppressor genes in pancreatic carcinoma, we performed loss of heterozygosity studies as well as mutation and expression analyses of SMAD4, SMAD2, and SMAD3 in 13 low-passage cell lines from 12 pancreatic carcinoma patients.]. 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:9892110
;
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:NP798110.RAm7wSk4LKMEOawoXdvhaLX0Vwxt37AiPW5lOFxgWKsbc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}