@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_head
{
this:
np:hasAssertion
dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_assertion
;
np:hasProvenance
dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_provenance
;
np:hasPublicationInfo
dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_assertion
a
np:Assertion
.
dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_provenance
a
np:Provenance
.
dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_assertion
{
miriam-gene:5551
a
ncit:C16612
.
lld:C0149925
a
ncit:C7057
.
dgn-gda:DGNbd3db3e9c3b07dcd3218d70532ce9187
sio:SIO_000628
miriam-gene:5551
,
lld:C0149925
;
a
sio:SIO_001121
.
}
dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_provenance
{
dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_assertion
dcterms:description
"[From this starting point, a P1 contig was developed for the region of 450 Kb that is common to the homozygous deletions seen in the SCLC lines NCI H740 and GLC20 and is also present in HA(3)BB9F, the suppressed A9 hybrid.]. 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:8957080
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:03+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}