@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE
> .
@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:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_head
{
this:
np:hasAssertion
dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_assertion
;
np:hasProvenance
dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_provenance
;
np:hasPublicationInfo
dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_assertion
a
np:Assertion
.
dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_provenance
a
np:Provenance
.
dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN59c4677b78fa6ba7dfec532833606cd2
sio:SIO_000628
miriam-gene:4360
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_provenance
{
dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_assertion
dcterms:description
"[To detect hereditary non-polyposis colorectal cancer (HNPCC) patients with a strategy combining clinical selection (patient age at onset of cancer less than 50 years or family history of HNPCC tumors) and microsatellite instability typing plus immunohistochemistry, leading to mismatch repair (MMR) germline mutation analysis.]. 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:16142001
;
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:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}