@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP268497.RA0Qm5-4AhXTKnZ_mDu2l5O5G-mkv17jeurcbhnZMgs5k
> .
@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:NP268497.RA0Qm5-4AhXTKnZ_mDu2l5O5G-mkv17jeurcbhnZMgs5k130_head
{
this:
np:hasAssertion
dgn-np:NP268497.RA0Qm5-4AhXTKnZ_mDu2l5O5G-mkv17jeurcbhnZMgs5k130_assertion
;
np:hasProvenance
dgn-np:NP268497.RA0Qm5-4AhXTKnZ_mDu2l5O5G-mkv17jeurcbhnZMgs5k130_provenance
;
np:hasPublicationInfo
dgn-np:NP268497.RA0Qm5-4AhXTKnZ_mDu2l5O5G-mkv17jeurcbhnZMgs5k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP268497.RA0Qm5-4AhXTKnZ_mDu2l5O5G-mkv17jeurcbhnZMgs5k130_assertion
a
np:Assertion
.
dgn-np:NP268497.RA0Qm5-4AhXTKnZ_mDu2l5O5G-mkv17jeurcbhnZMgs5k130_provenance
a
np:Provenance
.
dgn-np:NP268497.RA0Qm5-4AhXTKnZ_mDu2l5O5G-mkv17jeurcbhnZMgs5k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP268497.RA0Qm5-4AhXTKnZ_mDu2l5O5G-mkv17jeurcbhnZMgs5k130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0333983
a
ncit:C7057
.
dgn-gda:DGN7d1690e794e84a4b87dfc43f8927c1f1
sio:SIO_000628
miriam-gene:673
,
lld:C0333983
;
a
sio:SIO_001121
.
}
dgn-np:NP268497.RA0Qm5-4AhXTKnZ_mDu2l5O5G-mkv17jeurcbhnZMgs5k130_provenance
{
dgn-np:NP268497.RA0Qm5-4AhXTKnZ_mDu2l5O5G-mkv17jeurcbhnZMgs5k130_assertion
dcterms:description
"[The high incidence of BRAF mutations in HPs and SAs is consistent with the notion that the group of colorectal cancers carrying BRAF mutations may harbor most that have progressed through the HP-SA-carcinoma pathway.]. 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:12941809
;
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:NP268497.RA0Qm5-4AhXTKnZ_mDu2l5O5G-mkv17jeurcbhnZMgs5k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:30+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" .
}