@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP358267.RA263_wJgbOZ8y_bsjJFaItxCIBhQ6ge-lTBOQB3nVaUA
> .
@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:NP358267.RA263_wJgbOZ8y_bsjJFaItxCIBhQ6ge-lTBOQB3nVaUA130_head
{
this:
np:hasAssertion
dgn-np:NP358267.RA263_wJgbOZ8y_bsjJFaItxCIBhQ6ge-lTBOQB3nVaUA130_assertion
;
np:hasProvenance
dgn-np:NP358267.RA263_wJgbOZ8y_bsjJFaItxCIBhQ6ge-lTBOQB3nVaUA130_provenance
;
np:hasPublicationInfo
dgn-np:NP358267.RA263_wJgbOZ8y_bsjJFaItxCIBhQ6ge-lTBOQB3nVaUA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP358267.RA263_wJgbOZ8y_bsjJFaItxCIBhQ6ge-lTBOQB3nVaUA130_assertion
a
np:Assertion
.
dgn-np:NP358267.RA263_wJgbOZ8y_bsjJFaItxCIBhQ6ge-lTBOQB3nVaUA130_provenance
a
np:Provenance
.
dgn-np:NP358267.RA263_wJgbOZ8y_bsjJFaItxCIBhQ6ge-lTBOQB3nVaUA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP358267.RA263_wJgbOZ8y_bsjJFaItxCIBhQ6ge-lTBOQB3nVaUA130_assertion
{
miriam-gene:4595
a
ncit:C16612
.
lld:C0001430
a
ncit:C7057
.
dgn-gda:DGN2844c2a958f6b6e500c0de6694d756e0
sio:SIO_000628
miriam-gene:4595
,
lld:C0001430
;
a
sio:SIO_001121
.
}
dgn-np:NP358267.RA263_wJgbOZ8y_bsjJFaItxCIBhQ6ge-lTBOQB3nVaUA130_provenance
{
dgn-np:NP358267.RA263_wJgbOZ8y_bsjJFaItxCIBhQ6ge-lTBOQB3nVaUA130_assertion
dcterms:description
"[Because biallelic MYH mutations occur in patients with both high and low numbers of adenomas, we hypothesized that MYH is involved in the tumorigenesis of microsatellite stable colorectal cancers in patients without vertical transmission of disease and who fulfill the Bethesda guidelines.]. 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:16645203
;
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:NP358267.RA263_wJgbOZ8y_bsjJFaItxCIBhQ6ge-lTBOQB3nVaUA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:30+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" .
}