@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP871470.RA-LhCCQrzTqICINRnjjZXpuZo-IKj4aO9cQ4P6vyLlkU
> .
@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:NP871470.RA-LhCCQrzTqICINRnjjZXpuZo-IKj4aO9cQ4P6vyLlkU130_head
{
this:
np:hasAssertion
dgn-np:NP871470.RA-LhCCQrzTqICINRnjjZXpuZo-IKj4aO9cQ4P6vyLlkU130_assertion
;
np:hasProvenance
dgn-np:NP871470.RA-LhCCQrzTqICINRnjjZXpuZo-IKj4aO9cQ4P6vyLlkU130_provenance
;
np:hasPublicationInfo
dgn-np:NP871470.RA-LhCCQrzTqICINRnjjZXpuZo-IKj4aO9cQ4P6vyLlkU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP871470.RA-LhCCQrzTqICINRnjjZXpuZo-IKj4aO9cQ4P6vyLlkU130_assertion
a
np:Assertion
.
dgn-np:NP871470.RA-LhCCQrzTqICINRnjjZXpuZo-IKj4aO9cQ4P6vyLlkU130_provenance
a
np:Provenance
.
dgn-np:NP871470.RA-LhCCQrzTqICINRnjjZXpuZo-IKj4aO9cQ4P6vyLlkU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP871470.RA-LhCCQrzTqICINRnjjZXpuZo-IKj4aO9cQ4P6vyLlkU130_assertion
{
miriam-gene:978
a
ncit:C16612
.
lld:C0677932
a
ncit:C7057
.
dgn-gda:DGN4ca90f86724acfd283a3ef89fd95138b
sio:SIO_000628
miriam-gene:978
,
lld:C0677932
;
a
sio:SIO_001121
.
}
dgn-np:NP871470.RA-LhCCQrzTqICINRnjjZXpuZo-IKj4aO9cQ4P6vyLlkU130_provenance
{
dgn-np:NP871470.RA-LhCCQrzTqICINRnjjZXpuZo-IKj4aO9cQ4P6vyLlkU130_assertion
dcterms:description
"[This pilot study strongly suggests that UM patients are nearly five-times more likely to have progressive disease than patients with normal or low CDA activities, and that beside molecular events at the tumor level, upstream deregulations affecting drug disposition should be taken into account.]. 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:23837479
;
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:NP871470.RA-LhCCQrzTqICINRnjjZXpuZo-IKj4aO9cQ4P6vyLlkU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:53+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" .
}