@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP250843.RAb5lCr2efxO4B5R0jrVbITpnQbGXOX6BNLgnR0L4nU4U
> .
@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:NP250843.RAb5lCr2efxO4B5R0jrVbITpnQbGXOX6BNLgnR0L4nU4U130_head
{
this:
np:hasAssertion
dgn-np:NP250843.RAb5lCr2efxO4B5R0jrVbITpnQbGXOX6BNLgnR0L4nU4U130_assertion
;
np:hasProvenance
dgn-np:NP250843.RAb5lCr2efxO4B5R0jrVbITpnQbGXOX6BNLgnR0L4nU4U130_provenance
;
np:hasPublicationInfo
dgn-np:NP250843.RAb5lCr2efxO4B5R0jrVbITpnQbGXOX6BNLgnR0L4nU4U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP250843.RAb5lCr2efxO4B5R0jrVbITpnQbGXOX6BNLgnR0L4nU4U130_assertion
a
np:Assertion
.
dgn-np:NP250843.RAb5lCr2efxO4B5R0jrVbITpnQbGXOX6BNLgnR0L4nU4U130_provenance
a
np:Provenance
.
dgn-np:NP250843.RAb5lCr2efxO4B5R0jrVbITpnQbGXOX6BNLgnR0L4nU4U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP250843.RAb5lCr2efxO4B5R0jrVbITpnQbGXOX6BNLgnR0L4nU4U130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0007133
a
ncit:C7057
.
dgn-gda:DGNc0f430410d01a72b9d4440792e48fd9e
sio:SIO_000628
miriam-gene:673
,
lld:C0007133
;
a
sio:SIO_001121
.
}
dgn-np:NP250843.RAb5lCr2efxO4B5R0jrVbITpnQbGXOX6BNLgnR0L4nU4U130_provenance
{
dgn-np:NP250843.RAb5lCr2efxO4B5R0jrVbITpnQbGXOX6BNLgnR0L4nU4U130_assertion
dcterms:description
"[In summary, BRAF V600E mutation was occasionally observed in anaplastic carcinomas with papillary carcinoma, and the low frequency of BRAF V600E mutation in anaplastic carcinoma was thought to be due to the low frequency of anaplastic carcinomas with papillary 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:17453004
;
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:NP250843.RAb5lCr2efxO4B5R0jrVbITpnQbGXOX6BNLgnR0L4nU4U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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" .
}