@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP208770.RA8pnP4lEcC1AF19ZdfTPK-l-CVj3yHdg82-S_wQG3Fts
> .
@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:NP208770.RA8pnP4lEcC1AF19ZdfTPK-l-CVj3yHdg82-S_wQG3Fts130_head
{
this:
np:hasAssertion
dgn-np:NP208770.RA8pnP4lEcC1AF19ZdfTPK-l-CVj3yHdg82-S_wQG3Fts130_assertion
;
np:hasProvenance
dgn-np:NP208770.RA8pnP4lEcC1AF19ZdfTPK-l-CVj3yHdg82-S_wQG3Fts130_provenance
;
np:hasPublicationInfo
dgn-np:NP208770.RA8pnP4lEcC1AF19ZdfTPK-l-CVj3yHdg82-S_wQG3Fts130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP208770.RA8pnP4lEcC1AF19ZdfTPK-l-CVj3yHdg82-S_wQG3Fts130_assertion
a
np:Assertion
.
dgn-np:NP208770.RA8pnP4lEcC1AF19ZdfTPK-l-CVj3yHdg82-S_wQG3Fts130_provenance
a
np:Provenance
.
dgn-np:NP208770.RA8pnP4lEcC1AF19ZdfTPK-l-CVj3yHdg82-S_wQG3Fts130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP208770.RA8pnP4lEcC1AF19ZdfTPK-l-CVj3yHdg82-S_wQG3Fts130_assertion
{
miriam-gene:4254
a
ncit:C16612
.
lld:C0149925
a
ncit:C7057
.
dgn-gda:DGN2be631c8e7812c9832884054c86f8a2c
sio:SIO_000628
miriam-gene:4254
,
lld:C0149925
;
a
sio:SIO_001121
.
}
dgn-np:NP208770.RA8pnP4lEcC1AF19ZdfTPK-l-CVj3yHdg82-S_wQG3Fts130_provenance
{
dgn-np:NP208770.RA8pnP4lEcC1AF19ZdfTPK-l-CVj3yHdg82-S_wQG3Fts130_assertion
dcterms:description
"[Small cell lung cancer (SCLC) is characterized by multiple genetic alterations that include inactivation of the retinoblastoma protein (Rb), the establishment of several autocrine loops including that induced by coexpression of stem cell factor (SCF) and Kit, and the ectopic expression and activation of Src family kinases.]. 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:10910097
;
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:NP208770.RA8pnP4lEcC1AF19ZdfTPK-l-CVj3yHdg82-S_wQG3Fts130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:55+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" .
}