@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP825861.RAdqUGi7Cz0OkaQqQAi2BskOUYngzL5csO8IDfv-0gBzM
> .
@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:NP825861.RAdqUGi7Cz0OkaQqQAi2BskOUYngzL5csO8IDfv-0gBzM130_head
{
this:
np:hasAssertion
dgn-np:NP825861.RAdqUGi7Cz0OkaQqQAi2BskOUYngzL5csO8IDfv-0gBzM130_assertion
;
np:hasProvenance
dgn-np:NP825861.RAdqUGi7Cz0OkaQqQAi2BskOUYngzL5csO8IDfv-0gBzM130_provenance
;
np:hasPublicationInfo
dgn-np:NP825861.RAdqUGi7Cz0OkaQqQAi2BskOUYngzL5csO8IDfv-0gBzM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP825861.RAdqUGi7Cz0OkaQqQAi2BskOUYngzL5csO8IDfv-0gBzM130_assertion
a
np:Assertion
.
dgn-np:NP825861.RAdqUGi7Cz0OkaQqQAi2BskOUYngzL5csO8IDfv-0gBzM130_provenance
a
np:Provenance
.
dgn-np:NP825861.RAdqUGi7Cz0OkaQqQAi2BskOUYngzL5csO8IDfv-0gBzM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP825861.RAdqUGi7Cz0OkaQqQAi2BskOUYngzL5csO8IDfv-0gBzM130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0037274
a
ncit:C7057
.
dgn-gda:DGN64f0e101d55375b5260eba9acf66747b
sio:SIO_000628
miriam-gene:1956
,
lld:C0037274
;
a
sio:SIO_001121
.
}
dgn-np:NP825861.RAdqUGi7Cz0OkaQqQAi2BskOUYngzL5csO8IDfv-0gBzM130_provenance
{
dgn-np:NP825861.RAdqUGi7Cz0OkaQqQAi2BskOUYngzL5csO8IDfv-0gBzM130_assertion
dcterms:description
"[Skin disorders are among the most common adverse events related to treatment with epidermal growth factor receptor (EGFR) kinase inhibitors, and of these, erlotinib is known to cause more frequent and severe skin disease than other agents in this class.]. 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:21606217
;
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:NP825861.RAdqUGi7Cz0OkaQqQAi2BskOUYngzL5csO8IDfv-0gBzM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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" .
}