@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP264334.RAUnT5DWppAh07rLs5P0mN0-RwXSXhrdVlLaTiKjsHqFk
> .
@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:NP264334.RAUnT5DWppAh07rLs5P0mN0-RwXSXhrdVlLaTiKjsHqFk130_head
{
this:
np:hasAssertion
dgn-np:NP264334.RAUnT5DWppAh07rLs5P0mN0-RwXSXhrdVlLaTiKjsHqFk130_assertion
;
np:hasProvenance
dgn-np:NP264334.RAUnT5DWppAh07rLs5P0mN0-RwXSXhrdVlLaTiKjsHqFk130_provenance
;
np:hasPublicationInfo
dgn-np:NP264334.RAUnT5DWppAh07rLs5P0mN0-RwXSXhrdVlLaTiKjsHqFk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP264334.RAUnT5DWppAh07rLs5P0mN0-RwXSXhrdVlLaTiKjsHqFk130_assertion
a
np:Assertion
.
dgn-np:NP264334.RAUnT5DWppAh07rLs5P0mN0-RwXSXhrdVlLaTiKjsHqFk130_provenance
a
np:Provenance
.
dgn-np:NP264334.RAUnT5DWppAh07rLs5P0mN0-RwXSXhrdVlLaTiKjsHqFk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP264334.RAUnT5DWppAh07rLs5P0mN0-RwXSXhrdVlLaTiKjsHqFk130_assertion
{
miriam-gene:999
a
ncit:C16612
.
lld:C0699791
a
ncit:C7057
.
dgn-gda:DGNea9ccd3a3328e855774fb5ae2cdf4ff0
sio:SIO_000628
miriam-gene:999
,
lld:C0699791
;
a
sio:SIO_001121
.
}
dgn-np:NP264334.RAUnT5DWppAh07rLs5P0mN0-RwXSXhrdVlLaTiKjsHqFk130_provenance
{
dgn-np:NP264334.RAUnT5DWppAh07rLs5P0mN0-RwXSXhrdVlLaTiKjsHqFk130_assertion
dcterms:description
"[In the present study, we describe a Portuguese family with HDGC that was selected for CDH1 mutation screening after histological observation of the gastrectomy specimen of one member, who died at the age of 23 years from widely invasive diffuse gastric carcinoma.]. 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:15735979
;
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:NP264334.RAUnT5DWppAh07rLs5P0mN0-RwXSXhrdVlLaTiKjsHqFk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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" .
}