@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP244955.RAOkE9tddMaCRZuwmtbvjoBuW9712ItfgGC8xlA1xlyH8
> .
@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:NP244955.RAOkE9tddMaCRZuwmtbvjoBuW9712ItfgGC8xlA1xlyH8130_head
{
this:
np:hasAssertion
dgn-np:NP244955.RAOkE9tddMaCRZuwmtbvjoBuW9712ItfgGC8xlA1xlyH8130_assertion
;
np:hasProvenance
dgn-np:NP244955.RAOkE9tddMaCRZuwmtbvjoBuW9712ItfgGC8xlA1xlyH8130_provenance
;
np:hasPublicationInfo
dgn-np:NP244955.RAOkE9tddMaCRZuwmtbvjoBuW9712ItfgGC8xlA1xlyH8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP244955.RAOkE9tddMaCRZuwmtbvjoBuW9712ItfgGC8xlA1xlyH8130_assertion
a
np:Assertion
.
dgn-np:NP244955.RAOkE9tddMaCRZuwmtbvjoBuW9712ItfgGC8xlA1xlyH8130_provenance
a
np:Provenance
.
dgn-np:NP244955.RAOkE9tddMaCRZuwmtbvjoBuW9712ItfgGC8xlA1xlyH8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP244955.RAOkE9tddMaCRZuwmtbvjoBuW9712ItfgGC8xlA1xlyH8130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGNff94a69b1d8b9f70355deac8ed72e393
sio:SIO_000628
miriam-gene:3342
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP244955.RAOkE9tddMaCRZuwmtbvjoBuW9712ItfgGC8xlA1xlyH8130_provenance
{
dgn-np:NP244955.RAOkE9tddMaCRZuwmtbvjoBuW9712ItfgGC8xlA1xlyH8130_assertion
dcterms:description
"[Molecular genetic analysis, including DNA sequencing and CGH, revealed that both areas contained an identical NRAS Q61K mutation and had highly similar CGH profiles, including gains of chromosome 1q and losses of 1p, 4, 9, and 10, which are archetypical of melanoma.]. 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:21836492
;
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:NP244955.RAOkE9tddMaCRZuwmtbvjoBuW9712ItfgGC8xlA1xlyH8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:17+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" .
}