@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP738745.RAjj8dWawuURCCAB5JD5PurvpSDop79XpjqOxlCYFAnYs
> .
@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:NP738745.RAjj8dWawuURCCAB5JD5PurvpSDop79XpjqOxlCYFAnYs130_head
{
this:
np:hasAssertion
dgn-np:NP738745.RAjj8dWawuURCCAB5JD5PurvpSDop79XpjqOxlCYFAnYs130_assertion
;
np:hasProvenance
dgn-np:NP738745.RAjj8dWawuURCCAB5JD5PurvpSDop79XpjqOxlCYFAnYs130_provenance
;
np:hasPublicationInfo
dgn-np:NP738745.RAjj8dWawuURCCAB5JD5PurvpSDop79XpjqOxlCYFAnYs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP738745.RAjj8dWawuURCCAB5JD5PurvpSDop79XpjqOxlCYFAnYs130_assertion
a
np:Assertion
.
dgn-np:NP738745.RAjj8dWawuURCCAB5JD5PurvpSDop79XpjqOxlCYFAnYs130_provenance
a
np:Provenance
.
dgn-np:NP738745.RAjj8dWawuURCCAB5JD5PurvpSDop79XpjqOxlCYFAnYs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP738745.RAjj8dWawuURCCAB5JD5PurvpSDop79XpjqOxlCYFAnYs130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGN88a2aeb18d96bbd201c4ce31a4b207db
sio:SIO_000628
miriam-gene:673
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP738745.RAjj8dWawuURCCAB5JD5PurvpSDop79XpjqOxlCYFAnYs130_provenance
{
dgn-np:NP738745.RAjj8dWawuURCCAB5JD5PurvpSDop79XpjqOxlCYFAnYs130_assertion
dcterms:description
"[To clarify the extent of BRAF mutations in HNPCC colorectal carcinomas, which are typical mismatch repair deficient carcinomas, we compared the frequency of BRAF mutations between HNPCC, familial adenomatous polyposis (FAP) and sporadic cases.]. 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:15194222
;
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:NP738745.RAjj8dWawuURCCAB5JD5PurvpSDop79XpjqOxlCYFAnYs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:28+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" .
}