@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP268431.RAl2ryhiiLOiAYPV-Rc9zRHsNIDTN5ihzeFIqiGmUx81M
> .
@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:NP268431.RAl2ryhiiLOiAYPV-Rc9zRHsNIDTN5ihzeFIqiGmUx81M130_head
{
this:
np:hasAssertion
dgn-np:NP268431.RAl2ryhiiLOiAYPV-Rc9zRHsNIDTN5ihzeFIqiGmUx81M130_assertion
;
np:hasProvenance
dgn-np:NP268431.RAl2ryhiiLOiAYPV-Rc9zRHsNIDTN5ihzeFIqiGmUx81M130_provenance
;
np:hasPublicationInfo
dgn-np:NP268431.RAl2ryhiiLOiAYPV-Rc9zRHsNIDTN5ihzeFIqiGmUx81M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP268431.RAl2ryhiiLOiAYPV-Rc9zRHsNIDTN5ihzeFIqiGmUx81M130_assertion
a
np:Assertion
.
dgn-np:NP268431.RAl2ryhiiLOiAYPV-Rc9zRHsNIDTN5ihzeFIqiGmUx81M130_provenance
a
np:Provenance
.
dgn-np:NP268431.RAl2ryhiiLOiAYPV-Rc9zRHsNIDTN5ihzeFIqiGmUx81M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP268431.RAl2ryhiiLOiAYPV-Rc9zRHsNIDTN5ihzeFIqiGmUx81M130_assertion
{
miriam-gene:84700
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGN7e12ddc2cdb65ab31c424d053ad0c9a9
sio:SIO_000628
miriam-gene:84700
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP268431.RAl2ryhiiLOiAYPV-Rc9zRHsNIDTN5ihzeFIqiGmUx81M130_provenance
{
dgn-np:NP268431.RAl2ryhiiLOiAYPV-Rc9zRHsNIDTN5ihzeFIqiGmUx81M130_assertion
dcterms:description
"[Recently, we identified a novel myosin family gene, MYO18B, from the chromosome 22q12.1 region which shows frequent loss of heterozygosity in advanced lung cancer, and we found that this gene is inactivated in approximately 50% of lung cancers by deletions, mutations and methylation.]. 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:12741677
;
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:NP268431.RAl2ryhiiLOiAYPV-Rc9zRHsNIDTN5ihzeFIqiGmUx81M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:30+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" .
}