@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP926142.RAA7OzPWhPgQIhLxO2MooT0Jge9-hkFs1SMV27J3VRa9g
> .
@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:NP926142.RAA7OzPWhPgQIhLxO2MooT0Jge9-hkFs1SMV27J3VRa9g130_head
{
this:
np:hasAssertion
dgn-np:NP926142.RAA7OzPWhPgQIhLxO2MooT0Jge9-hkFs1SMV27J3VRa9g130_assertion
;
np:hasProvenance
dgn-np:NP926142.RAA7OzPWhPgQIhLxO2MooT0Jge9-hkFs1SMV27J3VRa9g130_provenance
;
np:hasPublicationInfo
dgn-np:NP926142.RAA7OzPWhPgQIhLxO2MooT0Jge9-hkFs1SMV27J3VRa9g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP926142.RAA7OzPWhPgQIhLxO2MooT0Jge9-hkFs1SMV27J3VRa9g130_assertion
a
np:Assertion
.
dgn-np:NP926142.RAA7OzPWhPgQIhLxO2MooT0Jge9-hkFs1SMV27J3VRa9g130_provenance
a
np:Provenance
.
dgn-np:NP926142.RAA7OzPWhPgQIhLxO2MooT0Jge9-hkFs1SMV27J3VRa9g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP926142.RAA7OzPWhPgQIhLxO2MooT0Jge9-hkFs1SMV27J3VRa9g130_assertion
{
miriam-gene:999
a
ncit:C16612
.
lld:C1335965
a
ncit:C7057
.
dgn-gda:DGN7e186ecdca866e64f0fc971bdab66124
sio:SIO_000628
miriam-gene:999
,
lld:C1335965
;
a
sio:SIO_001121
.
}
dgn-np:NP926142.RAA7OzPWhPgQIhLxO2MooT0Jge9-hkFs1SMV27J3VRa9g130_provenance
{
dgn-np:NP926142.RAA7OzPWhPgQIhLxO2MooT0Jge9-hkFs1SMV27J3VRa9g130_assertion
dcterms:description
"[The data show that asymptomatic patients with family history of HDGC and CDH1 mutation have high probability of having signet ring cell adenocarcinoma of the stomach that is not able to be diagnosed on endoscopy; when symptoms arise, the diagnosis can be made by endoscopy, but they have metastases and decreased survival.]. 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:21424370
;
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:NP926142.RAA7OzPWhPgQIhLxO2MooT0Jge9-hkFs1SMV27J3VRa9g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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" .
}