@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o
> .
@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:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_head
{
this:
np:hasAssertion
dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_assertion
;
np:hasProvenance
dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_provenance
;
np:hasPublicationInfo
dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_assertion
a
np:Assertion
.
dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_provenance
a
np:Provenance
.
dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN809a9b4a7cfc6d9f8a1868bbdfebf9e0
sio:SIO_000628
miriam-gene:1956
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_provenance
{
dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_assertion
dcterms:description
"[The histopathologic features of 10 myxoid adrenocortical neoplasms were analyzed, and epidermal growth factor receptor (EGFR) expression, EGFR gene copy number, and EGFR gene mutations in the 10 tumors were detected by using immunohistochemical analysis, fluorescence in situ hybridization, and the Scorpion Amplification Refractory Mutation System (DxS, Manchester, England), respectively.]. 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:22031318
;
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:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:56+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" .
}