@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP271919.RAAoWuptGo_XnTW3we8gwYohsSysN4AB4jloNrrC0aZxg
> .
@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:NP271919.RAAoWuptGo_XnTW3we8gwYohsSysN4AB4jloNrrC0aZxg130_head
{
this:
np:hasAssertion
dgn-np:NP271919.RAAoWuptGo_XnTW3we8gwYohsSysN4AB4jloNrrC0aZxg130_assertion
;
np:hasProvenance
dgn-np:NP271919.RAAoWuptGo_XnTW3we8gwYohsSysN4AB4jloNrrC0aZxg130_provenance
;
np:hasPublicationInfo
dgn-np:NP271919.RAAoWuptGo_XnTW3we8gwYohsSysN4AB4jloNrrC0aZxg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP271919.RAAoWuptGo_XnTW3we8gwYohsSysN4AB4jloNrrC0aZxg130_assertion
a
np:Assertion
.
dgn-np:NP271919.RAAoWuptGo_XnTW3we8gwYohsSysN4AB4jloNrrC0aZxg130_provenance
a
np:Provenance
.
dgn-np:NP271919.RAAoWuptGo_XnTW3we8gwYohsSysN4AB4jloNrrC0aZxg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP271919.RAAoWuptGo_XnTW3we8gwYohsSysN4AB4jloNrrC0aZxg130_assertion
{
miriam-gene:6597
a
ncit:C16612
.
lld:C0206743
a
ncit:C7057
.
dgn-gda:DGN3ff0b015a6f5ba093ee410de9add7d3f
sio:SIO_000628
miriam-gene:6597
,
lld:C0206743
;
a
sio:SIO_001121
.
}
dgn-np:NP271919.RAAoWuptGo_XnTW3we8gwYohsSysN4AB4jloNrrC0aZxg130_provenance
{
dgn-np:NP271919.RAAoWuptGo_XnTW3we8gwYohsSysN4AB4jloNrrC0aZxg130_assertion
dcterms:description
"[The SNF5 gene is biallelically inactivated in malignant rhabdoid tumors (MRTs) whereas BRG1 is mutated in cancer cell lines of several types, such as those of the breast, prostate, lung, pancreas and colon.]. 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:18437052
;
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:NP271919.RAAoWuptGo_XnTW3we8gwYohsSysN4AB4jloNrrC0aZxg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:33+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" .
}