@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc
> .
@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:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_head
{
this:
np:hasAssertion
dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_assertion
;
np:hasProvenance
dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_provenance
;
np:hasPublicationInfo
dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_assertion
a
np:Assertion
.
dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_provenance
a
np:Provenance
.
dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNcaa2595c44c2673d3c1462fe3347fcae
sio:SIO_000628
miriam-gene:673
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_provenance
{
dgn-np:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_assertion
dcterms:description
"[BRAF mutation testing has a role in (1) differentiating sporadic colorectal cancer from Lynch syndrome, (2) identifying cancers lacking BRAF mutation that are more likely to respond to epidermal growth factor receptor inhibitor therapy, and (3) conferring worse prognosis in colorectal cancer that is microsatellite stable.]. 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:20670148
;
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:NP154423.RAntHz6kndPWmBq39xmvI2-AjGYOam5eGYL5j3WyEVEEc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:22+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" .
}