@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP921558.RA1SrWWZ9vRAMQP4k9_ePvVlmQltCDpprLA9eoKW0Kw_I
> .
@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:NP921558.RA1SrWWZ9vRAMQP4k9_ePvVlmQltCDpprLA9eoKW0Kw_I130_head
{
this:
np:hasAssertion
dgn-np:NP921558.RA1SrWWZ9vRAMQP4k9_ePvVlmQltCDpprLA9eoKW0Kw_I130_assertion
;
np:hasProvenance
dgn-np:NP921558.RA1SrWWZ9vRAMQP4k9_ePvVlmQltCDpprLA9eoKW0Kw_I130_provenance
;
np:hasPublicationInfo
dgn-np:NP921558.RA1SrWWZ9vRAMQP4k9_ePvVlmQltCDpprLA9eoKW0Kw_I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP921558.RA1SrWWZ9vRAMQP4k9_ePvVlmQltCDpprLA9eoKW0Kw_I130_assertion
a
np:Assertion
.
dgn-np:NP921558.RA1SrWWZ9vRAMQP4k9_ePvVlmQltCDpprLA9eoKW0Kw_I130_provenance
a
np:Provenance
.
dgn-np:NP921558.RA1SrWWZ9vRAMQP4k9_ePvVlmQltCDpprLA9eoKW0Kw_I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP921558.RA1SrWWZ9vRAMQP4k9_ePvVlmQltCDpprLA9eoKW0Kw_I130_assertion
{
miriam-gene:6285
a
ncit:C16612
.
lld:C1334455
a
ncit:C7057
.
dgn-gda:DGN670ffa32f62a661f9b34a78709b9a07a
sio:SIO_000628
miriam-gene:6285
,
lld:C1334455
;
a
sio:SIO_001121
.
}
dgn-np:NP921558.RA1SrWWZ9vRAMQP4k9_ePvVlmQltCDpprLA9eoKW0Kw_I130_provenance
{
dgn-np:NP921558.RA1SrWWZ9vRAMQP4k9_ePvVlmQltCDpprLA9eoKW0Kw_I130_assertion
dcterms:description
"[They found the lesional cells of SH to be epithelial membrane antigen (EMA) positive (21 of 21 cases), to be keratin positive only infrequently and focally (six of 21), and to be nonreactive for carcinoembryonic antigen, S-100, smooth muscle actin, and CD34.]. 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:10716159
;
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:NP921558.RA1SrWWZ9vRAMQP4k9_ePvVlmQltCDpprLA9eoKW0Kw_I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:25+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" .
}