@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP911355.RAO-1DlH2wKVjCZ8WM6aQUWNFhcnMOXCg3PA_pbyXFWE0
> .
@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:NP911355.RAO-1DlH2wKVjCZ8WM6aQUWNFhcnMOXCg3PA_pbyXFWE0130_head
{
this:
np:hasAssertion
dgn-np:NP911355.RAO-1DlH2wKVjCZ8WM6aQUWNFhcnMOXCg3PA_pbyXFWE0130_assertion
;
np:hasProvenance
dgn-np:NP911355.RAO-1DlH2wKVjCZ8WM6aQUWNFhcnMOXCg3PA_pbyXFWE0130_provenance
;
np:hasPublicationInfo
dgn-np:NP911355.RAO-1DlH2wKVjCZ8WM6aQUWNFhcnMOXCg3PA_pbyXFWE0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP911355.RAO-1DlH2wKVjCZ8WM6aQUWNFhcnMOXCg3PA_pbyXFWE0130_assertion
a
np:Assertion
.
dgn-np:NP911355.RAO-1DlH2wKVjCZ8WM6aQUWNFhcnMOXCg3PA_pbyXFWE0130_provenance
a
np:Provenance
.
dgn-np:NP911355.RAO-1DlH2wKVjCZ8WM6aQUWNFhcnMOXCg3PA_pbyXFWE0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP911355.RAO-1DlH2wKVjCZ8WM6aQUWNFhcnMOXCg3PA_pbyXFWE0130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0205969
a
ncit:C7057
.
dgn-gda:DGN55a957525441c8d3f7e0cf8470c73d3b
sio:SIO_000628
miriam-gene:1956
,
lld:C0205969
;
a
sio:SIO_001121
.
}
dgn-np:NP911355.RAO-1DlH2wKVjCZ8WM6aQUWNFhcnMOXCg3PA_pbyXFWE0130_provenance
{
dgn-np:NP911355.RAO-1DlH2wKVjCZ8WM6aQUWNFhcnMOXCg3PA_pbyXFWE0130_assertion
dcterms:description
"[We have investigated 20 different subtypes of thymomas (type A, AB, and B3) and thymic carcinomas for mutations in exons 18, 19, 20, and 21 of the EGFR gene and performed immunohistochemistry for EGFR.]. 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:16919868
;
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:NP911355.RAO-1DlH2wKVjCZ8WM6aQUWNFhcnMOXCg3PA_pbyXFWE0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:19+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" .
}