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http://rdf.disgenet.org/nanopublications.trig#NP585351.RAXa-prPvO8NuT2wILMcZB7ZA1svtrTkKOOtiO1IVsyXA
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP585351.RAXa-prPvO8NuT2wILMcZB7ZA1svtrTkKOOtiO1IVsyXA130_assertion
;
np:hasProvenance
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dgn-np:NP585351.RAXa-prPvO8NuT2wILMcZB7ZA1svtrTkKOOtiO1IVsyXA130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP585351.RAXa-prPvO8NuT2wILMcZB7ZA1svtrTkKOOtiO1IVsyXA130_assertion
a
np:Assertion
.
dgn-np:NP585351.RAXa-prPvO8NuT2wILMcZB7ZA1svtrTkKOOtiO1IVsyXA130_provenance
a
np:Provenance
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dgn-np:NP585351.RAXa-prPvO8NuT2wILMcZB7ZA1svtrTkKOOtiO1IVsyXA130_publicationInfo
a
np:PublicationInfo
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dgn-np:NP585351.RAXa-prPvO8NuT2wILMcZB7ZA1svtrTkKOOtiO1IVsyXA130_assertion
{
miriam-gene:3265
a
ncit:C16612
.
lld:C1833921
a
ncit:C7057
.
dgn-gda:DGNd810c0e6bf67af42abd9b79ea3a47f2f
sio:SIO_000628
miriam-gene:3265
,
lld:C1833921
;
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.
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dgn-np:NP585351.RAXa-prPvO8NuT2wILMcZB7ZA1svtrTkKOOtiO1IVsyXA130_provenance
{
dgn-np:NP585351.RAXa-prPvO8NuT2wILMcZB7ZA1svtrTkKOOtiO1IVsyXA130_assertion
dcterms:description
"[We performed PCR amplification and sequencing analysis of the three mutational hotspots (codons 12, 13, and 61) of the H-, K-, and N-RAS genes, and of the mutational hotspot (codon 600) and exon 11 of the BRAF gene in 65 sporadic MTC, of which 40 were RET positive and 25 were RET negative.]. 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:21325462
;
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:NP585351.RAXa-prPvO8NuT2wILMcZB7ZA1svtrTkKOOtiO1IVsyXA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:52+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
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pav:authoredBy
<
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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