@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48533.RAas1nvXJYCOGsas2eEPptxjI9sIfg2F3hGbuhMTxBkyk
> .
@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:NP48533.RAas1nvXJYCOGsas2eEPptxjI9sIfg2F3hGbuhMTxBkyk130_head
{
this:
np:hasAssertion
dgn-np:NP48533.RAas1nvXJYCOGsas2eEPptxjI9sIfg2F3hGbuhMTxBkyk130_assertion
;
np:hasProvenance
dgn-np:NP48533.RAas1nvXJYCOGsas2eEPptxjI9sIfg2F3hGbuhMTxBkyk130_provenance
;
np:hasPublicationInfo
dgn-np:NP48533.RAas1nvXJYCOGsas2eEPptxjI9sIfg2F3hGbuhMTxBkyk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48533.RAas1nvXJYCOGsas2eEPptxjI9sIfg2F3hGbuhMTxBkyk130_assertion
a
np:Assertion
.
dgn-np:NP48533.RAas1nvXJYCOGsas2eEPptxjI9sIfg2F3hGbuhMTxBkyk130_provenance
a
np:Provenance
.
dgn-np:NP48533.RAas1nvXJYCOGsas2eEPptxjI9sIfg2F3hGbuhMTxBkyk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48533.RAas1nvXJYCOGsas2eEPptxjI9sIfg2F3hGbuhMTxBkyk130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN79f0ddee746bd36f9fa466aaf1d86a2d
sio:SIO_000628
miriam-gene:324
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP48533.RAas1nvXJYCOGsas2eEPptxjI9sIfg2F3hGbuhMTxBkyk130_provenance
{
dgn-np:NP48533.RAas1nvXJYCOGsas2eEPptxjI9sIfg2F3hGbuhMTxBkyk130_assertion
dcterms:description
"[Genomic DNA, which was extracted from peripheral blood lymphocytes of 22 FAP patients and the normal colon tissues of 43 sporadic colorectal cancers, were examined for mutations in exon15 of the APC gene by using PCR-TNT T7 Quick Coupled Tanscription/Translation System.]. 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:16201232
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48533.RAas1nvXJYCOGsas2eEPptxjI9sIfg2F3hGbuhMTxBkyk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}