@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP295525.RA-vyutBJfCmUJlZKI6YMqdXn2kpeWKL0Icw_WHhLPC2c
> .
@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:NP295525.RA-vyutBJfCmUJlZKI6YMqdXn2kpeWKL0Icw_WHhLPC2c130_head
{
this:
np:hasAssertion
dgn-np:NP295525.RA-vyutBJfCmUJlZKI6YMqdXn2kpeWKL0Icw_WHhLPC2c130_assertion
;
np:hasProvenance
dgn-np:NP295525.RA-vyutBJfCmUJlZKI6YMqdXn2kpeWKL0Icw_WHhLPC2c130_provenance
;
np:hasPublicationInfo
dgn-np:NP295525.RA-vyutBJfCmUJlZKI6YMqdXn2kpeWKL0Icw_WHhLPC2c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295525.RA-vyutBJfCmUJlZKI6YMqdXn2kpeWKL0Icw_WHhLPC2c130_assertion
a
np:Assertion
.
dgn-np:NP295525.RA-vyutBJfCmUJlZKI6YMqdXn2kpeWKL0Icw_WHhLPC2c130_provenance
a
np:Provenance
.
dgn-np:NP295525.RA-vyutBJfCmUJlZKI6YMqdXn2kpeWKL0Icw_WHhLPC2c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP295525.RA-vyutBJfCmUJlZKI6YMqdXn2kpeWKL0Icw_WHhLPC2c130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0699790
a
ncit:C7057
.
dgn-gda:DGNec78325943e3bd662df64edb6b79ec11
sio:SIO_000628
miriam-gene:4360
,
lld:C0699790
;
a
sio:SIO_001121
.
}
dgn-np:NP295525.RA-vyutBJfCmUJlZKI6YMqdXn2kpeWKL0Icw_WHhLPC2c130_provenance
{
dgn-np:NP295525.RA-vyutBJfCmUJlZKI6YMqdXn2kpeWKL0Icw_WHhLPC2c130_assertion
dcterms:description
"[In this report, we show that such hybrid cell lines can also be a valuable tool in the study of the mutated MMR proteins, in particular the variants found in hereditary nonpolyposis colon cancer families that carry missense mutations and where it is unclear whether they predispose to colon cancer.]. 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:11691782
;
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:NP295525.RA-vyutBJfCmUJlZKI6YMqdXn2kpeWKL0Icw_WHhLPC2c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}