@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP425979.RAMnYrT8H36jURhurWOH1e7NhDS-mHTldXtQJbJwE8e4o
> .
@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:NP425979.RAMnYrT8H36jURhurWOH1e7NhDS-mHTldXtQJbJwE8e4o130_head
{
this:
np:hasAssertion
dgn-np:NP425979.RAMnYrT8H36jURhurWOH1e7NhDS-mHTldXtQJbJwE8e4o130_assertion
;
np:hasProvenance
dgn-np:NP425979.RAMnYrT8H36jURhurWOH1e7NhDS-mHTldXtQJbJwE8e4o130_provenance
;
np:hasPublicationInfo
dgn-np:NP425979.RAMnYrT8H36jURhurWOH1e7NhDS-mHTldXtQJbJwE8e4o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP425979.RAMnYrT8H36jURhurWOH1e7NhDS-mHTldXtQJbJwE8e4o130_assertion
a
np:Assertion
.
dgn-np:NP425979.RAMnYrT8H36jURhurWOH1e7NhDS-mHTldXtQJbJwE8e4o130_provenance
a
np:Provenance
.
dgn-np:NP425979.RAMnYrT8H36jURhurWOH1e7NhDS-mHTldXtQJbJwE8e4o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP425979.RAMnYrT8H36jURhurWOH1e7NhDS-mHTldXtQJbJwE8e4o130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGNefa1c35d0a0a1c7c269d15ea416c4b81
sio:SIO_000628
miriam-gene:3342
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP425979.RAMnYrT8H36jURhurWOH1e7NhDS-mHTldXtQJbJwE8e4o130_provenance
{
dgn-np:NP425979.RAMnYrT8H36jURhurWOH1e7NhDS-mHTldXtQJbJwE8e4o130_assertion
dcterms:description
"[The rapidly expanding database of CGH publications already covers about 1500 tumors and is beginning to reveal genetic abnormalities that are characteristic of certain tumor types or stages of tumor progression.]. 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:9351342
;
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:NP425979.RAMnYrT8H36jURhurWOH1e7NhDS-mHTldXtQJbJwE8e4o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:12+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" .
}