@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP203493.RAmJpYWmZ8T9tU1bjRiafrHLi4q7RAIrqfNeBWdUNuwQ0
> .
@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:NP203493.RAmJpYWmZ8T9tU1bjRiafrHLi4q7RAIrqfNeBWdUNuwQ0130_head
{
this:
np:hasAssertion
dgn-np:NP203493.RAmJpYWmZ8T9tU1bjRiafrHLi4q7RAIrqfNeBWdUNuwQ0130_assertion
;
np:hasProvenance
dgn-np:NP203493.RAmJpYWmZ8T9tU1bjRiafrHLi4q7RAIrqfNeBWdUNuwQ0130_provenance
;
np:hasPublicationInfo
dgn-np:NP203493.RAmJpYWmZ8T9tU1bjRiafrHLi4q7RAIrqfNeBWdUNuwQ0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP203493.RAmJpYWmZ8T9tU1bjRiafrHLi4q7RAIrqfNeBWdUNuwQ0130_assertion
a
np:Assertion
.
dgn-np:NP203493.RAmJpYWmZ8T9tU1bjRiafrHLi4q7RAIrqfNeBWdUNuwQ0130_provenance
a
np:Provenance
.
dgn-np:NP203493.RAmJpYWmZ8T9tU1bjRiafrHLi4q7RAIrqfNeBWdUNuwQ0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP203493.RAmJpYWmZ8T9tU1bjRiafrHLi4q7RAIrqfNeBWdUNuwQ0130_assertion
{
miriam-gene:2010
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN3f9d46f35566c30df23a000c0b840565
sio:SIO_000628
miriam-gene:2010
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP203493.RAmJpYWmZ8T9tU1bjRiafrHLi4q7RAIrqfNeBWdUNuwQ0130_provenance
{
dgn-np:NP203493.RAmJpYWmZ8T9tU1bjRiafrHLi4q7RAIrqfNeBWdUNuwQ0130_assertion
dcterms:description
"[The aim of this study was to evaluate the sensitivity of the Enzymatic Mutation Detection (EMD) assay in HNPCC using genomic DNA samples with known gene alterations in MLH1 and MSH2.]. 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:10874307
;
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:NP203493.RAmJpYWmZ8T9tU1bjRiafrHLi4q7RAIrqfNeBWdUNuwQ0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:52+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" .
}