@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP164797.RAxjHWmKgt0jrFaWNouFzLuvd8RKAWXrPMDxa_q7ulhvE
> .
@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:NP164797.RAxjHWmKgt0jrFaWNouFzLuvd8RKAWXrPMDxa_q7ulhvE130_head
{
this:
np:hasAssertion
dgn-np:NP164797.RAxjHWmKgt0jrFaWNouFzLuvd8RKAWXrPMDxa_q7ulhvE130_assertion
;
np:hasProvenance
dgn-np:NP164797.RAxjHWmKgt0jrFaWNouFzLuvd8RKAWXrPMDxa_q7ulhvE130_provenance
;
np:hasPublicationInfo
dgn-np:NP164797.RAxjHWmKgt0jrFaWNouFzLuvd8RKAWXrPMDxa_q7ulhvE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP164797.RAxjHWmKgt0jrFaWNouFzLuvd8RKAWXrPMDxa_q7ulhvE130_assertion
a
np:Assertion
.
dgn-np:NP164797.RAxjHWmKgt0jrFaWNouFzLuvd8RKAWXrPMDxa_q7ulhvE130_provenance
a
np:Provenance
.
dgn-np:NP164797.RAxjHWmKgt0jrFaWNouFzLuvd8RKAWXrPMDxa_q7ulhvE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP164797.RAxjHWmKgt0jrFaWNouFzLuvd8RKAWXrPMDxa_q7ulhvE130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNf7cf56ca5dd70fa6b3e07d86f539971d
sio:SIO_000628
miriam-gene:4436
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP164797.RAxjHWmKgt0jrFaWNouFzLuvd8RKAWXrPMDxa_q7ulhvE130_provenance
{
dgn-np:NP164797.RAxjHWmKgt0jrFaWNouFzLuvd8RKAWXrPMDxa_q7ulhvE130_assertion
dcterms:description
"[The risk of developing cancer of the ovaries, stomach, and brain was also higher in the MSH2 mutation carriers than in the MLH1 mutation carriers, but the difference was not statistically significant.]. 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:11600610
;
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:NP164797.RAxjHWmKgt0jrFaWNouFzLuvd8RKAWXrPMDxa_q7ulhvE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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" .
}