@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP888139.RAcwarK9Voum1Z1UGknRar5ruxGQXMmYt786l2wlFA3Sg
> .
@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:NP888139.RAcwarK9Voum1Z1UGknRar5ruxGQXMmYt786l2wlFA3Sg130_head
{
this:
np:hasAssertion
dgn-np:NP888139.RAcwarK9Voum1Z1UGknRar5ruxGQXMmYt786l2wlFA3Sg130_assertion
;
np:hasProvenance
dgn-np:NP888139.RAcwarK9Voum1Z1UGknRar5ruxGQXMmYt786l2wlFA3Sg130_provenance
;
np:hasPublicationInfo
dgn-np:NP888139.RAcwarK9Voum1Z1UGknRar5ruxGQXMmYt786l2wlFA3Sg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP888139.RAcwarK9Voum1Z1UGknRar5ruxGQXMmYt786l2wlFA3Sg130_assertion
a
np:Assertion
.
dgn-np:NP888139.RAcwarK9Voum1Z1UGknRar5ruxGQXMmYt786l2wlFA3Sg130_provenance
a
np:Provenance
.
dgn-np:NP888139.RAcwarK9Voum1Z1UGknRar5ruxGQXMmYt786l2wlFA3Sg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP888139.RAcwarK9Voum1Z1UGknRar5ruxGQXMmYt786l2wlFA3Sg130_assertion
{
miriam-gene:4831
a
ncit:C16612
.
lld:C0686619
a
ncit:C7057
.
dgn-gda:DGNc9e1d8d1a9cc15c32f54274c100b0df2
sio:SIO_000628
miriam-gene:4831
,
lld:C0686619
;
a
sio:SIO_001121
.
}
dgn-np:NP888139.RAcwarK9Voum1Z1UGknRar5ruxGQXMmYt786l2wlFA3Sg130_provenance
{
dgn-np:NP888139.RAcwarK9Voum1Z1UGknRar5ruxGQXMmYt786l2wlFA3Sg130_assertion
dcterms:description
"[NM23.H2 was always more highly expressed than NM23.H1, and reduced expression of NM23.H1 but not NM23.H2 was concordant with the presence of lymph node metastasis or local invasiveness of the primary tumor.]. 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:9036878
;
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:NP888139.RAcwarK9Voum1Z1UGknRar5ruxGQXMmYt786l2wlFA3Sg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:05+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" .
}