@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP167637.RA5wJjnqat9MRIwnjW5GK1ybpPt_rTUoB1aXyY2Yd4KBA
> .
@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:NP167637.RA5wJjnqat9MRIwnjW5GK1ybpPt_rTUoB1aXyY2Yd4KBA130_head
{
this:
np:hasAssertion
dgn-np:NP167637.RA5wJjnqat9MRIwnjW5GK1ybpPt_rTUoB1aXyY2Yd4KBA130_assertion
;
np:hasProvenance
dgn-np:NP167637.RA5wJjnqat9MRIwnjW5GK1ybpPt_rTUoB1aXyY2Yd4KBA130_provenance
;
np:hasPublicationInfo
dgn-np:NP167637.RA5wJjnqat9MRIwnjW5GK1ybpPt_rTUoB1aXyY2Yd4KBA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP167637.RA5wJjnqat9MRIwnjW5GK1ybpPt_rTUoB1aXyY2Yd4KBA130_assertion
a
np:Assertion
.
dgn-np:NP167637.RA5wJjnqat9MRIwnjW5GK1ybpPt_rTUoB1aXyY2Yd4KBA130_provenance
a
np:Provenance
.
dgn-np:NP167637.RA5wJjnqat9MRIwnjW5GK1ybpPt_rTUoB1aXyY2Yd4KBA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP167637.RA5wJjnqat9MRIwnjW5GK1ybpPt_rTUoB1aXyY2Yd4KBA130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN7d37f6186599a7d2c68c04dd8e7c2919
sio:SIO_000628
miriam-gene:4292
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP167637.RA5wJjnqat9MRIwnjW5GK1ybpPt_rTUoB1aXyY2Yd4KBA130_provenance
{
dgn-np:NP167637.RA5wJjnqat9MRIwnjW5GK1ybpPt_rTUoB1aXyY2Yd4KBA130_assertion
dcterms:description
"[A new mechanism leading to cancer has been delineated in the last two years when genes whose mutations cause susceptibility to hereditary nonpolyposis colorectal cancer, HNPCC, have been mapped, cloned, and characterized.]. 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:8825478
;
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:NP167637.RA5wJjnqat9MRIwnjW5GK1ybpPt_rTUoB1aXyY2Yd4KBA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}