@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP78935.RAvI4VeoVbPCjKsHNGRkCwbz_cbL3jn2DSV6UCroL0Py8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP78935.RAvI4VeoVbPCjKsHNGRkCwbz_cbL3jn2DSV6UCroL0Py8130_head
{
this:
np:hasAssertion
dgn-np:NP78935.RAvI4VeoVbPCjKsHNGRkCwbz_cbL3jn2DSV6UCroL0Py8130_assertion
;
np:hasProvenance
dgn-np:NP78935.RAvI4VeoVbPCjKsHNGRkCwbz_cbL3jn2DSV6UCroL0Py8130_provenance
;
np:hasPublicationInfo
dgn-np:NP78935.RAvI4VeoVbPCjKsHNGRkCwbz_cbL3jn2DSV6UCroL0Py8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP78935.RAvI4VeoVbPCjKsHNGRkCwbz_cbL3jn2DSV6UCroL0Py8130_assertion
a
np:Assertion
.
dgn-np:NP78935.RAvI4VeoVbPCjKsHNGRkCwbz_cbL3jn2DSV6UCroL0Py8130_provenance
a
np:Provenance
.
dgn-np:NP78935.RAvI4VeoVbPCjKsHNGRkCwbz_cbL3jn2DSV6UCroL0Py8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP78935.RAvI4VeoVbPCjKsHNGRkCwbz_cbL3jn2DSV6UCroL0Py8130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN4b5ae40562eb50b5cfdf12f238a31351
sio:SIO_000628
miriam-gene:3845
,
lld:C0242379
;
a
sio:SIO_001122
.
}
dgn-np:NP78935.RAvI4VeoVbPCjKsHNGRkCwbz_cbL3jn2DSV6UCroL0Py8130_provenance
{
dgn-np:NP78935.RAvI4VeoVbPCjKsHNGRkCwbz_cbL3jn2DSV6UCroL0Py8130_assertion
dcterms:description
"[Cetuximab might add benefit in treatment after failure of gefitinib, regardless of EGFR mutational status. Treatment with cetuximab should be further explored, even in patients who have previously received gefitinib treatment.]. 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:20630828
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP78935.RAvI4VeoVbPCjKsHNGRkCwbz_cbL3jn2DSV6UCroL0Py8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:23+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}