@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP216784.RAZIxrFX3XJOcwf3pJpbtB_ByMTsuF4P2vuUtrOoVIBkU
> .
@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:NP216784.RAZIxrFX3XJOcwf3pJpbtB_ByMTsuF4P2vuUtrOoVIBkU130_head
{
this:
np:hasAssertion
dgn-np:NP216784.RAZIxrFX3XJOcwf3pJpbtB_ByMTsuF4P2vuUtrOoVIBkU130_assertion
;
np:hasProvenance
dgn-np:NP216784.RAZIxrFX3XJOcwf3pJpbtB_ByMTsuF4P2vuUtrOoVIBkU130_provenance
;
np:hasPublicationInfo
dgn-np:NP216784.RAZIxrFX3XJOcwf3pJpbtB_ByMTsuF4P2vuUtrOoVIBkU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216784.RAZIxrFX3XJOcwf3pJpbtB_ByMTsuF4P2vuUtrOoVIBkU130_assertion
a
np:Assertion
.
dgn-np:NP216784.RAZIxrFX3XJOcwf3pJpbtB_ByMTsuF4P2vuUtrOoVIBkU130_provenance
a
np:Provenance
.
dgn-np:NP216784.RAZIxrFX3XJOcwf3pJpbtB_ByMTsuF4P2vuUtrOoVIBkU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216784.RAZIxrFX3XJOcwf3pJpbtB_ByMTsuF4P2vuUtrOoVIBkU130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGN3d33f986b44bc16e9e9d0849a1f0ffe5
sio:SIO_000628
miriam-gene:1956
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP216784.RAZIxrFX3XJOcwf3pJpbtB_ByMTsuF4P2vuUtrOoVIBkU130_provenance
{
dgn-np:NP216784.RAZIxrFX3XJOcwf3pJpbtB_ByMTsuF4P2vuUtrOoVIBkU130_assertion
dcterms:description
"[This includes the susceptibility factors, an association between genetic changes in EGFR pathway and tyrosine kinase inhibitors, the role of gene hypermethylation and genetic profiling, as well as different molecular aspects 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:15800676
;
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:NP216784.RAZIxrFX3XJOcwf3pJpbtB_ByMTsuF4P2vuUtrOoVIBkU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}