@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk
> .
@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:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_head
{
this:
np:hasAssertion
dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_assertion
;
np:hasProvenance
dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_provenance
;
np:hasPublicationInfo
dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_assertion
a
np:Assertion
.
dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_provenance
a
np:Provenance
.
dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0149925
a
ncit:C7057
.
dgn-gda:DGN5ed09dbed5dc4bd950ba5d4d523d4bf4
sio:SIO_000628
miriam-gene:324
,
lld:C0149925
;
a
sio:SIO_001121
.
}
dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_provenance
{
dgn-np:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_assertion
dcterms:description
"[Seven cases were informative for both genes, loss of heterozygosity occurred for both genes in five, one retained heterozygosity for both, and one SCLC had loss of heterozygosity for APC but not for MCC.]. 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:1348017
;
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:NP379226.RAtDBzKVwjtD8jmhsBlKK5ZyRn_Xw2n9I-qZCNSkOo3Kk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:44+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" .
}