@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP549803.RA4lySzOn3irNXmqvlMNUhtiSV78nmwPuaHiD8gmrjN9M
> .
@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:NP549803.RA4lySzOn3irNXmqvlMNUhtiSV78nmwPuaHiD8gmrjN9M130_head
{
this:
np:hasAssertion
dgn-np:NP549803.RA4lySzOn3irNXmqvlMNUhtiSV78nmwPuaHiD8gmrjN9M130_assertion
;
np:hasProvenance
dgn-np:NP549803.RA4lySzOn3irNXmqvlMNUhtiSV78nmwPuaHiD8gmrjN9M130_provenance
;
np:hasPublicationInfo
dgn-np:NP549803.RA4lySzOn3irNXmqvlMNUhtiSV78nmwPuaHiD8gmrjN9M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP549803.RA4lySzOn3irNXmqvlMNUhtiSV78nmwPuaHiD8gmrjN9M130_assertion
a
np:Assertion
.
dgn-np:NP549803.RA4lySzOn3irNXmqvlMNUhtiSV78nmwPuaHiD8gmrjN9M130_provenance
a
np:Provenance
.
dgn-np:NP549803.RA4lySzOn3irNXmqvlMNUhtiSV78nmwPuaHiD8gmrjN9M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP549803.RA4lySzOn3irNXmqvlMNUhtiSV78nmwPuaHiD8gmrjN9M130_assertion
{
miriam-gene:2778
a
ncit:C16612
.
lld:C0027819
a
ncit:C7057
.
dgn-gda:DGNbb5ff93666d874ebf13d7c105def5a95
sio:SIO_000628
miriam-gene:2778
,
lld:C0027819
;
a
sio:SIO_001121
.
}
dgn-np:NP549803.RA4lySzOn3irNXmqvlMNUhtiSV78nmwPuaHiD8gmrjN9M130_provenance
{
dgn-np:NP549803.RA4lySzOn3irNXmqvlMNUhtiSV78nmwPuaHiD8gmrjN9M130_assertion
dcterms:description
"[Pancreatic endocrine tumours (14 out of 25), pheochromocytomas (19 out of 19), and neuroblastomas (seven out of 14) expressed NESP55, with the same strong labelling pattern in both benign and malignant tumours.]. 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:12771991
;
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:NP549803.RA4lySzOn3irNXmqvlMNUhtiSV78nmwPuaHiD8gmrjN9M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:31+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" .
}