@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP166586.RA_PEfA_CzYxBaEDlEFSmnmM7q00kd2I-m8wtbW81BHtk
> .
@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:NP166586.RA_PEfA_CzYxBaEDlEFSmnmM7q00kd2I-m8wtbW81BHtk130_head
{
this:
np:hasAssertion
dgn-np:NP166586.RA_PEfA_CzYxBaEDlEFSmnmM7q00kd2I-m8wtbW81BHtk130_assertion
;
np:hasProvenance
dgn-np:NP166586.RA_PEfA_CzYxBaEDlEFSmnmM7q00kd2I-m8wtbW81BHtk130_provenance
;
np:hasPublicationInfo
dgn-np:NP166586.RA_PEfA_CzYxBaEDlEFSmnmM7q00kd2I-m8wtbW81BHtk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP166586.RA_PEfA_CzYxBaEDlEFSmnmM7q00kd2I-m8wtbW81BHtk130_assertion
a
np:Assertion
.
dgn-np:NP166586.RA_PEfA_CzYxBaEDlEFSmnmM7q00kd2I-m8wtbW81BHtk130_provenance
a
np:Provenance
.
dgn-np:NP166586.RA_PEfA_CzYxBaEDlEFSmnmM7q00kd2I-m8wtbW81BHtk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP166586.RA_PEfA_CzYxBaEDlEFSmnmM7q00kd2I-m8wtbW81BHtk130_assertion
{
miriam-gene:238
a
ncit:C16612
.
lld:C0001418
a
ncit:C7057
.
dgn-gda:DGN005fd20913981be79284885bf4987c2f
sio:SIO_000628
miriam-gene:238
,
lld:C0001418
;
a
sio:SIO_001121
.
}
dgn-np:NP166586.RA_PEfA_CzYxBaEDlEFSmnmM7q00kd2I-m8wtbW81BHtk130_provenance
{
dgn-np:NP166586.RA_PEfA_CzYxBaEDlEFSmnmM7q00kd2I-m8wtbW81BHtk130_assertion
dcterms:description
"[The two essential requirements for pathologic specimens in the era of personalized therapies for non-small cell lung carcinoma (NSCLC) are accurate subtyping as adenocarcinoma (ADC) versus squamous cell carcinoma (SqCC) and suitability for EGFR molecular testing, as well as for testing of other oncogenes such as EML4-ALK and KRAS.]. 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:23423768
;
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:NP166586.RA_PEfA_CzYxBaEDlEFSmnmM7q00kd2I-m8wtbW81BHtk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}