@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP645419.RASluAPkxEof9Cy0XqY5bzll4k0nCGciKrMr1kHLKfYPM
> .
@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:NP645419.RASluAPkxEof9Cy0XqY5bzll4k0nCGciKrMr1kHLKfYPM130_head
{
this:
np:hasAssertion
dgn-np:NP645419.RASluAPkxEof9Cy0XqY5bzll4k0nCGciKrMr1kHLKfYPM130_assertion
;
np:hasProvenance
dgn-np:NP645419.RASluAPkxEof9Cy0XqY5bzll4k0nCGciKrMr1kHLKfYPM130_provenance
;
np:hasPublicationInfo
dgn-np:NP645419.RASluAPkxEof9Cy0XqY5bzll4k0nCGciKrMr1kHLKfYPM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP645419.RASluAPkxEof9Cy0XqY5bzll4k0nCGciKrMr1kHLKfYPM130_assertion
a
np:Assertion
.
dgn-np:NP645419.RASluAPkxEof9Cy0XqY5bzll4k0nCGciKrMr1kHLKfYPM130_provenance
a
np:Provenance
.
dgn-np:NP645419.RASluAPkxEof9Cy0XqY5bzll4k0nCGciKrMr1kHLKfYPM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP645419.RASluAPkxEof9Cy0XqY5bzll4k0nCGciKrMr1kHLKfYPM130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0032000
a
ncit:C7057
.
dgn-gda:DGN5f8fbd23707f8f34d23ee38e8dccff35
sio:SIO_000628
miriam-gene:3342
,
lld:C0032000
;
a
sio:SIO_001121
.
}
dgn-np:NP645419.RASluAPkxEof9Cy0XqY5bzll4k0nCGciKrMr1kHLKfYPM130_provenance
{
dgn-np:NP645419.RASluAPkxEof9Cy0XqY5bzll4k0nCGciKrMr1kHLKfYPM130_assertion
dcterms:description
"[Because the value of karyotyping is limited by the technical problems related to cytogenetic methods, we studied the spectrum of chromosomal imbalances associated with pituitary adenoma using comparative genomic hybridization (CGH).]. 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:14558668
;
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:NP645419.RASluAPkxEof9Cy0XqY5bzll4k0nCGciKrMr1kHLKfYPM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:29+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" .
}