@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0
> .
@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:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_head
{
this:
np:hasAssertion
dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_assertion
;
np:hasProvenance
dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_provenance
;
np:hasPublicationInfo
dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_assertion
a
np:Assertion
.
dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_provenance
a
np:Provenance
.
dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_assertion
{
miriam-gene:8581
a
ncit:C16612
.
lld:C0268074
a
ncit:C7057
.
dgn-gda:DGN4c8c2aa752b84163bde1c874e22994d3
sio:SIO_000628
miriam-gene:8581
,
lld:C0268074
;
a
sio:SIO_001121
.
}
dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_provenance
{
dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_assertion
dcterms:description
"[The concordance between the molecular and ICC tests applied to preoperative samples, measured by Cohen's kappa, was not uniformly good, which likely reflected sampling errors, heterogeneity of E48 antigen expression, or stochastic effects.]. 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:14614011
;
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:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:59+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" .
}