@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP559245.RAIrJJvCg_7hxst6VxtOjT9bt361Z41I2lc2VMtIcerfw
> .
@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:NP559245.RAIrJJvCg_7hxst6VxtOjT9bt361Z41I2lc2VMtIcerfw130_head
{
this:
np:hasAssertion
dgn-np:NP559245.RAIrJJvCg_7hxst6VxtOjT9bt361Z41I2lc2VMtIcerfw130_assertion
;
np:hasProvenance
dgn-np:NP559245.RAIrJJvCg_7hxst6VxtOjT9bt361Z41I2lc2VMtIcerfw130_provenance
;
np:hasPublicationInfo
dgn-np:NP559245.RAIrJJvCg_7hxst6VxtOjT9bt361Z41I2lc2VMtIcerfw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP559245.RAIrJJvCg_7hxst6VxtOjT9bt361Z41I2lc2VMtIcerfw130_assertion
a
np:Assertion
.
dgn-np:NP559245.RAIrJJvCg_7hxst6VxtOjT9bt361Z41I2lc2VMtIcerfw130_provenance
a
np:Provenance
.
dgn-np:NP559245.RAIrJJvCg_7hxst6VxtOjT9bt361Z41I2lc2VMtIcerfw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP559245.RAIrJJvCg_7hxst6VxtOjT9bt361Z41I2lc2VMtIcerfw130_assertion
{
miriam-gene:57045
a
ncit:C16612
.
lld:C1458155
a
ncit:C7057
.
dgn-gda:DGN3720ed413d72c15aa69de82b5b1bbdfd
sio:SIO_000628
miriam-gene:57045
,
lld:C1458155
;
a
sio:SIO_001121
.
}
dgn-np:NP559245.RAIrJJvCg_7hxst6VxtOjT9bt361Z41I2lc2VMtIcerfw130_provenance
{
dgn-np:NP559245.RAIrJJvCg_7hxst6VxtOjT9bt361Z41I2lc2VMtIcerfw130_assertion
dcterms:description
"[The CGH data from AA were compared to published lists of 41 TSG and oncogenes in Caucasians and 68 cancer genes, proposed via systematic sequencing for somatic mutations in colon and breast tumors.]. 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:22879877
;
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:NP559245.RAIrJJvCg_7hxst6VxtOjT9bt361Z41I2lc2VMtIcerfw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:37+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" .
}