@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP348842.RABFKGoCy3ckPIaXUJ4qTVpNalsi8qeArGyqctwR-24CI
> .
@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:NP348842.RABFKGoCy3ckPIaXUJ4qTVpNalsi8qeArGyqctwR-24CI130_head
{
this:
np:hasAssertion
dgn-np:NP348842.RABFKGoCy3ckPIaXUJ4qTVpNalsi8qeArGyqctwR-24CI130_assertion
;
np:hasProvenance
dgn-np:NP348842.RABFKGoCy3ckPIaXUJ4qTVpNalsi8qeArGyqctwR-24CI130_provenance
;
np:hasPublicationInfo
dgn-np:NP348842.RABFKGoCy3ckPIaXUJ4qTVpNalsi8qeArGyqctwR-24CI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP348842.RABFKGoCy3ckPIaXUJ4qTVpNalsi8qeArGyqctwR-24CI130_assertion
a
np:Assertion
.
dgn-np:NP348842.RABFKGoCy3ckPIaXUJ4qTVpNalsi8qeArGyqctwR-24CI130_provenance
a
np:Provenance
.
dgn-np:NP348842.RABFKGoCy3ckPIaXUJ4qTVpNalsi8qeArGyqctwR-24CI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP348842.RABFKGoCy3ckPIaXUJ4qTVpNalsi8qeArGyqctwR-24CI130_assertion
{
miriam-gene:1630
a
ncit:C16612
.
lld:C1333991
a
ncit:C7057
.
dgn-gda:DGN4394a55de8abab393295a1c726bc6303
sio:SIO_000628
miriam-gene:1630
,
lld:C1333991
;
a
sio:SIO_001121
.
}
dgn-np:NP348842.RABFKGoCy3ckPIaXUJ4qTVpNalsi8qeArGyqctwR-24CI130_provenance
{
dgn-np:NP348842.RABFKGoCy3ckPIaXUJ4qTVpNalsi8qeArGyqctwR-24CI130_assertion
dcterms:description
"[Because both ovarian and colon cancer are features of Lynch syndrome II, which has been provisionally mapped to chromosome 18, we hypothesized that loss of heterozygosity at the DCC locus may also occur in ovarian neoplasia.]. 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:1594239
;
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:NP348842.RABFKGoCy3ckPIaXUJ4qTVpNalsi8qeArGyqctwR-24CI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:25+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" .
}