@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8
> .
@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:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_head
{
this:
np:hasAssertion
dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_assertion
;
np:hasProvenance
dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_provenance
;
np:hasPublicationInfo
dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_assertion
a
np:Assertion
.
dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_provenance
a
np:Provenance
.
dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN9c7c2dd4e43ce549e3709130dbb7352b
sio:SIO_000628
miriam-gene:673
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_provenance
{
dgn-np:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_assertion
dcterms:description
"[The association of BRAF V600E mutation and the presence of the CpG island methylator phenotype (CIMP) and microsatellite instability (MSI) often confound analysis of BRAF mutation status and survival in colorectal carcinoma.]. 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:22314188
;
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:NP193129.RADblFpfulq6u4bN6kY7USZ_VDQvPDc7zo5-CL3_nIVA8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:46+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" .
}