@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP141962.RAnka1cRMiRkAridVWIAlUkU4pX7-bFsARCsvHBTX8zKc
> .
@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:NP141962.RAnka1cRMiRkAridVWIAlUkU4pX7-bFsARCsvHBTX8zKc130_head
{
this:
np:hasAssertion
dgn-np:NP141962.RAnka1cRMiRkAridVWIAlUkU4pX7-bFsARCsvHBTX8zKc130_assertion
;
np:hasProvenance
dgn-np:NP141962.RAnka1cRMiRkAridVWIAlUkU4pX7-bFsARCsvHBTX8zKc130_provenance
;
np:hasPublicationInfo
dgn-np:NP141962.RAnka1cRMiRkAridVWIAlUkU4pX7-bFsARCsvHBTX8zKc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP141962.RAnka1cRMiRkAridVWIAlUkU4pX7-bFsARCsvHBTX8zKc130_assertion
a
np:Assertion
.
dgn-np:NP141962.RAnka1cRMiRkAridVWIAlUkU4pX7-bFsARCsvHBTX8zKc130_provenance
a
np:Provenance
.
dgn-np:NP141962.RAnka1cRMiRkAridVWIAlUkU4pX7-bFsARCsvHBTX8zKc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP141962.RAnka1cRMiRkAridVWIAlUkU4pX7-bFsARCsvHBTX8zKc130_assertion
{
miriam-gene:999
a
ncit:C16612
.
lld:C0206692
a
ncit:C7057
.
dgn-gda:DGNcab1166b850c55dcd19f47890f816183
sio:SIO_000628
miriam-gene:999
,
lld:C0206692
;
a
sio:SIO_001122
.
}
dgn-np:NP141962.RAnka1cRMiRkAridVWIAlUkU4pX7-bFsARCsvHBTX8zKc130_provenance
{
dgn-np:NP141962.RAnka1cRMiRkAridVWIAlUkU4pX7-bFsARCsvHBTX8zKc130_assertion
dcterms:description
"[In most hereditary cancer syndromes, like hereditory diffuse gastric cancer and lobular carcinoma of the breast, multiple organ sites are affected by cancer and have been shown to be associated with germline mutations in CDH1 at 16q22.1.]. 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:18046629
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP141962.RAnka1cRMiRkAridVWIAlUkU4pX7-bFsARCsvHBTX8zKc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:14+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" .
}