@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg
> .
@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:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_head
{
this:
np:hasAssertion
dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_assertion
;
np:hasProvenance
dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance
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np:hasPublicationInfo
dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_assertion
a
np:Assertion
.
dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance
a
np:Provenance
.
dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_assertion
{
miriam-gene:57697
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN66da302c5b8c9f81c2a5b251401f9ac0
sio:SIO_000628
miriam-gene:57697
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance
{
dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_assertion
dcterms:description
"[We sought somatic mutations in the corresponding genes in the CRCs of the patients harboring the germline lesions and found biallelic inactivation of FANCM, LAMB4, PTCHD3, LAMC3, and TREX2, potentially implicating these genes as tumor suppressors.]. 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:23585368
;
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:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:09+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" .
}