@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE
> .
@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:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_head
{
this:
np:hasAssertion
dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_assertion
;
np:hasProvenance
dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_provenance
;
np:hasPublicationInfo
dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_assertion
a
np:Assertion
.
dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_provenance
a
np:Provenance
.
dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_assertion
{
miriam-gene:7294
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN256e4fe7950b6fe69e37b827cced45a8
sio:SIO_000628
miriam-gene:7294
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_provenance
{
dgn-np:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_assertion
dcterms:description
"[Somatic mutations in the tyrosine kinase (TK) domain of the epidermal growth factor receptor (EGFR) gene in lung cancers have generated enormous interest, because they predict for sensitivity to TK inhibitors (TKIs).]. 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:16231326
;
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:NP350816.RAM8Is2qZr_q6AOZIgnn8RjrVH2hnqcEPS7O22rJkrNXE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:26+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" .
}