@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP811577.RAWu3ecBcVT_aV1T9W2VeIW-lFgrfFRh9XrqeDyehPie0
> .
@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:NP811577.RAWu3ecBcVT_aV1T9W2VeIW-lFgrfFRh9XrqeDyehPie0130_head
{
this:
np:hasAssertion
dgn-np:NP811577.RAWu3ecBcVT_aV1T9W2VeIW-lFgrfFRh9XrqeDyehPie0130_assertion
;
np:hasProvenance
dgn-np:NP811577.RAWu3ecBcVT_aV1T9W2VeIW-lFgrfFRh9XrqeDyehPie0130_provenance
;
np:hasPublicationInfo
dgn-np:NP811577.RAWu3ecBcVT_aV1T9W2VeIW-lFgrfFRh9XrqeDyehPie0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP811577.RAWu3ecBcVT_aV1T9W2VeIW-lFgrfFRh9XrqeDyehPie0130_assertion
a
np:Assertion
.
dgn-np:NP811577.RAWu3ecBcVT_aV1T9W2VeIW-lFgrfFRh9XrqeDyehPie0130_provenance
a
np:Provenance
.
dgn-np:NP811577.RAWu3ecBcVT_aV1T9W2VeIW-lFgrfFRh9XrqeDyehPie0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP811577.RAWu3ecBcVT_aV1T9W2VeIW-lFgrfFRh9XrqeDyehPie0130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0024814
a
ncit:C7057
.
dgn-gda:DGN4c474a9a41f7495d4011e324c9d5dd90
sio:SIO_000628
miriam-gene:4436
,
lld:C0024814
;
a
sio:SIO_001121
.
}
dgn-np:NP811577.RAWu3ecBcVT_aV1T9W2VeIW-lFgrfFRh9XrqeDyehPie0130_provenance
{
dgn-np:NP811577.RAWu3ecBcVT_aV1T9W2VeIW-lFgrfFRh9XrqeDyehPie0130_assertion
dcterms:description
"[Whereas the HNPCC-related tumors demonstrated MSI phenotype, loss of MSH2 protein expression, and frameshift mutations in several of the 13 target genes analyzed, the kidney cancer displayed MSS phenotype, normal MMR protein expression, and no frameshift mutation in target genes.]. 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:16639607
;
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:NP811577.RAWu3ecBcVT_aV1T9W2VeIW-lFgrfFRh9XrqeDyehPie0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:17+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" .
}