@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP343272.RAsX9mK_4N1nCuOo9zkSQD7W_-E9_SXP1vB-UoCrULO4Y
> .
@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:NP343272.RAsX9mK_4N1nCuOo9zkSQD7W_-E9_SXP1vB-UoCrULO4Y130_head
{
this:
np:hasAssertion
dgn-np:NP343272.RAsX9mK_4N1nCuOo9zkSQD7W_-E9_SXP1vB-UoCrULO4Y130_assertion
;
np:hasProvenance
dgn-np:NP343272.RAsX9mK_4N1nCuOo9zkSQD7W_-E9_SXP1vB-UoCrULO4Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP343272.RAsX9mK_4N1nCuOo9zkSQD7W_-E9_SXP1vB-UoCrULO4Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP343272.RAsX9mK_4N1nCuOo9zkSQD7W_-E9_SXP1vB-UoCrULO4Y130_assertion
a
np:Assertion
.
dgn-np:NP343272.RAsX9mK_4N1nCuOo9zkSQD7W_-E9_SXP1vB-UoCrULO4Y130_provenance
a
np:Provenance
.
dgn-np:NP343272.RAsX9mK_4N1nCuOo9zkSQD7W_-E9_SXP1vB-UoCrULO4Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP343272.RAsX9mK_4N1nCuOo9zkSQD7W_-E9_SXP1vB-UoCrULO4Y130_assertion
{
miriam-gene:7294
a
ncit:C16612
.
lld:C0027819
a
ncit:C7057
.
dgn-gda:DGN4e4d856c0fc0a4d8e13061e12748fdd0
sio:SIO_000628
miriam-gene:7294
,
lld:C0027819
;
a
sio:SIO_001121
.
}
dgn-np:NP343272.RAsX9mK_4N1nCuOo9zkSQD7W_-E9_SXP1vB-UoCrULO4Y130_provenance
{
dgn-np:NP343272.RAsX9mK_4N1nCuOo9zkSQD7W_-E9_SXP1vB-UoCrULO4Y130_assertion
dcterms:description
"[Included in these genetic alterations are mutations in the kinase domain of the anaplastic lymphoma kinase (ALK) receptor tyrosine kinase (RTK), which have been found in both somatic and familial neuroblastoma.]. 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:23104988
;
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:NP343272.RAsX9mK_4N1nCuOo9zkSQD7W_-E9_SXP1vB-UoCrULO4Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:22+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" .
}