@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP513252.RAp8Xwp6PU4sL7GrD1zJBQQVR_Bvuvu2oVljK6AeIYv9U
> .
@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:NP513252.RAp8Xwp6PU4sL7GrD1zJBQQVR_Bvuvu2oVljK6AeIYv9U130_head
{
this:
np:hasAssertion
dgn-np:NP513252.RAp8Xwp6PU4sL7GrD1zJBQQVR_Bvuvu2oVljK6AeIYv9U130_assertion
;
np:hasProvenance
dgn-np:NP513252.RAp8Xwp6PU4sL7GrD1zJBQQVR_Bvuvu2oVljK6AeIYv9U130_provenance
;
np:hasPublicationInfo
dgn-np:NP513252.RAp8Xwp6PU4sL7GrD1zJBQQVR_Bvuvu2oVljK6AeIYv9U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP513252.RAp8Xwp6PU4sL7GrD1zJBQQVR_Bvuvu2oVljK6AeIYv9U130_assertion
a
np:Assertion
.
dgn-np:NP513252.RAp8Xwp6PU4sL7GrD1zJBQQVR_Bvuvu2oVljK6AeIYv9U130_provenance
a
np:Provenance
.
dgn-np:NP513252.RAp8Xwp6PU4sL7GrD1zJBQQVR_Bvuvu2oVljK6AeIYv9U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP513252.RAp8Xwp6PU4sL7GrD1zJBQQVR_Bvuvu2oVljK6AeIYv9U130_assertion
{
miriam-gene:4610
a
ncit:C16612
.
lld:C0024623
a
ncit:C7057
.
dgn-gda:DGN1af9c011665b251045299783de58e48a
sio:SIO_000628
miriam-gene:4610
,
lld:C0024623
;
a
sio:SIO_001121
.
}
dgn-np:NP513252.RAp8Xwp6PU4sL7GrD1zJBQQVR_Bvuvu2oVljK6AeIYv9U130_provenance
{
dgn-np:NP513252.RAp8Xwp6PU4sL7GrD1zJBQQVR_Bvuvu2oVljK6AeIYv9U130_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:NP513252.RAp8Xwp6PU4sL7GrD1zJBQQVR_Bvuvu2oVljK6AeIYv9U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:06+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" .
}