@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP765435.RA1efhQ-S9TrhQg7RPIG3WPIL8qzGQNpBD2rcRH_Od5Ac
> .
@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:NP765435.RA1efhQ-S9TrhQg7RPIG3WPIL8qzGQNpBD2rcRH_Od5Ac130_head
{
this:
np:hasAssertion
dgn-np:NP765435.RA1efhQ-S9TrhQg7RPIG3WPIL8qzGQNpBD2rcRH_Od5Ac130_assertion
;
np:hasProvenance
dgn-np:NP765435.RA1efhQ-S9TrhQg7RPIG3WPIL8qzGQNpBD2rcRH_Od5Ac130_provenance
;
np:hasPublicationInfo
dgn-np:NP765435.RA1efhQ-S9TrhQg7RPIG3WPIL8qzGQNpBD2rcRH_Od5Ac130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP765435.RA1efhQ-S9TrhQg7RPIG3WPIL8qzGQNpBD2rcRH_Od5Ac130_assertion
a
np:Assertion
.
dgn-np:NP765435.RA1efhQ-S9TrhQg7RPIG3WPIL8qzGQNpBD2rcRH_Od5Ac130_provenance
a
np:Provenance
.
dgn-np:NP765435.RA1efhQ-S9TrhQg7RPIG3WPIL8qzGQNpBD2rcRH_Od5Ac130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP765435.RA1efhQ-S9TrhQg7RPIG3WPIL8qzGQNpBD2rcRH_Od5Ac130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0024623
a
ncit:C7057
.
dgn-gda:DGN6090728a25bd79875177a3a00413965b
sio:SIO_000628
miriam-gene:4436
,
lld:C0024623
;
a
sio:SIO_001121
.
}
dgn-np:NP765435.RA1efhQ-S9TrhQg7RPIG3WPIL8qzGQNpBD2rcRH_Od5Ac130_provenance
{
dgn-np:NP765435.RA1efhQ-S9TrhQg7RPIG3WPIL8qzGQNpBD2rcRH_Od5Ac130_assertion
dcterms:description
"[Although polymorphisms in DNA mismatch repair (MMR) gene MSH2 have been associated with risks of many cancers, little is known about their etiology role in gastric cancer (GC) and the potential interacting role with lifestyle factors known to damage DNA.]. 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:22386861
;
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:NP765435.RA1efhQ-S9TrhQg7RPIG3WPIL8qzGQNpBD2rcRH_Od5Ac130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:43+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" .
}