@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP762308.RA0pMDWORpmcFH4ERxn1vhrng0QgSJ-xKP8z8vBQxJfMo
> .
@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:NP762308.RA0pMDWORpmcFH4ERxn1vhrng0QgSJ-xKP8z8vBQxJfMo130_head
{
this:
np:hasAssertion
dgn-np:NP762308.RA0pMDWORpmcFH4ERxn1vhrng0QgSJ-xKP8z8vBQxJfMo130_assertion
;
np:hasProvenance
dgn-np:NP762308.RA0pMDWORpmcFH4ERxn1vhrng0QgSJ-xKP8z8vBQxJfMo130_provenance
;
np:hasPublicationInfo
dgn-np:NP762308.RA0pMDWORpmcFH4ERxn1vhrng0QgSJ-xKP8z8vBQxJfMo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP762308.RA0pMDWORpmcFH4ERxn1vhrng0QgSJ-xKP8z8vBQxJfMo130_assertion
a
np:Assertion
.
dgn-np:NP762308.RA0pMDWORpmcFH4ERxn1vhrng0QgSJ-xKP8z8vBQxJfMo130_provenance
a
np:Provenance
.
dgn-np:NP762308.RA0pMDWORpmcFH4ERxn1vhrng0QgSJ-xKP8z8vBQxJfMo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP762308.RA0pMDWORpmcFH4ERxn1vhrng0QgSJ-xKP8z8vBQxJfMo130_assertion
{
miriam-gene:9612
a
ncit:C16612
.
lld:C0007120
a
ncit:C7057
.
dgn-gda:DGN423473cc2adcbfa23a513aa140b21667
sio:SIO_000628
miriam-gene:9612
,
lld:C0007120
;
a
sio:SIO_001121
.
}
dgn-np:NP762308.RA0pMDWORpmcFH4ERxn1vhrng0QgSJ-xKP8z8vBQxJfMo130_provenance
{
dgn-np:NP762308.RA0pMDWORpmcFH4ERxn1vhrng0QgSJ-xKP8z8vBQxJfMo130_assertion
dcterms:description
"[In this study, we first simulated normal cell contamination to determine the heterogeneity tolerance of array CGH and then validated this detection sensitivity model on cancer specimens using the newly developed submegabase resolution tiling-set (SMRT) array, which spans the human genome with 32,433 overlapping BAC clones.]. 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:15885505
;
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:NP762308.RA0pMDWORpmcFH4ERxn1vhrng0QgSJ-xKP8z8vBQxJfMo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:41+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" .
}