@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP480609.RAE5WlbHVnyRkt5q7EI1-fta6p5I-UJ8Jn4s1lU74MyZo
> .
@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:NP480609.RAE5WlbHVnyRkt5q7EI1-fta6p5I-UJ8Jn4s1lU74MyZo130_head
{
this:
np:hasAssertion
dgn-np:NP480609.RAE5WlbHVnyRkt5q7EI1-fta6p5I-UJ8Jn4s1lU74MyZo130_assertion
;
np:hasProvenance
dgn-np:NP480609.RAE5WlbHVnyRkt5q7EI1-fta6p5I-UJ8Jn4s1lU74MyZo130_provenance
;
np:hasPublicationInfo
dgn-np:NP480609.RAE5WlbHVnyRkt5q7EI1-fta6p5I-UJ8Jn4s1lU74MyZo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP480609.RAE5WlbHVnyRkt5q7EI1-fta6p5I-UJ8Jn4s1lU74MyZo130_assertion
a
np:Assertion
.
dgn-np:NP480609.RAE5WlbHVnyRkt5q7EI1-fta6p5I-UJ8Jn4s1lU74MyZo130_provenance
a
np:Provenance
.
dgn-np:NP480609.RAE5WlbHVnyRkt5q7EI1-fta6p5I-UJ8Jn4s1lU74MyZo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP480609.RAE5WlbHVnyRkt5q7EI1-fta6p5I-UJ8Jn4s1lU74MyZo130_assertion
{
miriam-gene:54802
a
ncit:C16612
.
lld:C0024623
a
ncit:C7057
.
dgn-gda:DGN70e00e6557c0f71cea968c723321e50f
sio:SIO_000628
miriam-gene:54802
,
lld:C0024623
;
a
sio:SIO_001121
.
}
dgn-np:NP480609.RAE5WlbHVnyRkt5q7EI1-fta6p5I-UJ8Jn4s1lU74MyZo130_provenance
{
dgn-np:NP480609.RAE5WlbHVnyRkt5q7EI1-fta6p5I-UJ8Jn4s1lU74MyZo130_assertion
dcterms:description
"[This is believed to be the first report that several tagging SNPs and haplotypes in TRIT1, MYCL1 and MFSD2A region are significantly associated with risk and clinicopathological features of gastric cancer in a Chinese population.]. 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:23349019
;
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:NP480609.RAE5WlbHVnyRkt5q7EI1-fta6p5I-UJ8Jn4s1lU74MyZo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:47+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" .
}