@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA
> .
@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:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_head
{
this:
np:hasAssertion
dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_assertion
;
np:hasProvenance
dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_provenance
;
np:hasPublicationInfo
dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_assertion
a
np:Assertion
.
dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_provenance
a
np:Provenance
.
dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0205698
a
ncit:C7057
.
dgn-gda:DGNfafc483644167d3e7b19935c3501c469
sio:SIO_000628
miriam-gene:1956
,
lld:C0205698
;
a
sio:SIO_001121
.
}
dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_provenance
{
dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_assertion
dcterms:description
"[EFGR mutations, including 12 cases of EGFR exon 19 deletion and 11 cases of exon 21 point mutation, were present in 21 patients with adenocarcinomas, one with squamous cell carcinoma, and one with undifferentiated carcinoma.]. 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:22006985
;
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:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:06+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" .
}