@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP145484.RAO7TwNM0Ub6lF1bKXWnreadc7s4wOpQEEsmCepFrBZA0
> .
@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:NP145484.RAO7TwNM0Ub6lF1bKXWnreadc7s4wOpQEEsmCepFrBZA0130_head
{
this:
np:hasAssertion
dgn-np:NP145484.RAO7TwNM0Ub6lF1bKXWnreadc7s4wOpQEEsmCepFrBZA0130_assertion
;
np:hasProvenance
dgn-np:NP145484.RAO7TwNM0Ub6lF1bKXWnreadc7s4wOpQEEsmCepFrBZA0130_provenance
;
np:hasPublicationInfo
dgn-np:NP145484.RAO7TwNM0Ub6lF1bKXWnreadc7s4wOpQEEsmCepFrBZA0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP145484.RAO7TwNM0Ub6lF1bKXWnreadc7s4wOpQEEsmCepFrBZA0130_assertion
a
np:Assertion
.
dgn-np:NP145484.RAO7TwNM0Ub6lF1bKXWnreadc7s4wOpQEEsmCepFrBZA0130_provenance
a
np:Provenance
.
dgn-np:NP145484.RAO7TwNM0Ub6lF1bKXWnreadc7s4wOpQEEsmCepFrBZA0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP145484.RAO7TwNM0Ub6lF1bKXWnreadc7s4wOpQEEsmCepFrBZA0130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C0017185
a
ncit:C7057
.
dgn-gda:DGNc791c5efe90c132b651151e905d3eba4
sio:SIO_000628
miriam-gene:4292
,
lld:C0017185
;
a
sio:SIO_001122
.
}
dgn-np:NP145484.RAO7TwNM0Ub6lF1bKXWnreadc7s4wOpQEEsmCepFrBZA0130_provenance
{
dgn-np:NP145484.RAO7TwNM0Ub6lF1bKXWnreadc7s4wOpQEEsmCepFrBZA0130_assertion
dcterms:description
"[This work availably evaluated the functional consequences of some missense mutations not previously determined in the hMLH1 gene and might be useful for the clinical diagnosis of hereditary gastrointestinal cancer, especially in East Asians ]. 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:18094436
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP145484.RAO7TwNM0Ub6lF1bKXWnreadc7s4wOpQEEsmCepFrBZA0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:16+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" .
}