@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP159509.RA2Wuev82c9QtaSRhusz6AsCpXcY31rT2tqUxYoepw86E
> .
@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:NP159509.RA2Wuev82c9QtaSRhusz6AsCpXcY31rT2tqUxYoepw86E130_head
{
this:
np:hasAssertion
dgn-np:NP159509.RA2Wuev82c9QtaSRhusz6AsCpXcY31rT2tqUxYoepw86E130_assertion
;
np:hasProvenance
dgn-np:NP159509.RA2Wuev82c9QtaSRhusz6AsCpXcY31rT2tqUxYoepw86E130_provenance
;
np:hasPublicationInfo
dgn-np:NP159509.RA2Wuev82c9QtaSRhusz6AsCpXcY31rT2tqUxYoepw86E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP159509.RA2Wuev82c9QtaSRhusz6AsCpXcY31rT2tqUxYoepw86E130_assertion
a
np:Assertion
.
dgn-np:NP159509.RA2Wuev82c9QtaSRhusz6AsCpXcY31rT2tqUxYoepw86E130_provenance
a
np:Provenance
.
dgn-np:NP159509.RA2Wuev82c9QtaSRhusz6AsCpXcY31rT2tqUxYoepw86E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP159509.RA2Wuev82c9QtaSRhusz6AsCpXcY31rT2tqUxYoepw86E130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN259fe9cee8ef02146cf0324ba775e264
sio:SIO_000628
miriam-gene:4360
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP159509.RA2Wuev82c9QtaSRhusz6AsCpXcY31rT2tqUxYoepw86E130_provenance
{
dgn-np:NP159509.RA2Wuev82c9QtaSRhusz6AsCpXcY31rT2tqUxYoepw86E130_assertion
dcterms:description
"[The discovery of DNA mismatch repair (MMR) genes, inclusive of hMSH2, hMLH1, hPMS2, and hMSH6, has enabled the identification of who has and who does not have inordinately increased susceptibility to CRC as well as a litany of extracolonic cancers.]. 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:10630171
;
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:NP159509.RA2Wuev82c9QtaSRhusz6AsCpXcY31rT2tqUxYoepw86E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+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" .
}