@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP864893.RAopgSiYsHfUJD0tHl9L-evr19pB9_6xgC_slpL1KMgfU
> .
@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:NP864893.RAopgSiYsHfUJD0tHl9L-evr19pB9_6xgC_slpL1KMgfU130_head
{
this:
np:hasAssertion
dgn-np:NP864893.RAopgSiYsHfUJD0tHl9L-evr19pB9_6xgC_slpL1KMgfU130_assertion
;
np:hasProvenance
dgn-np:NP864893.RAopgSiYsHfUJD0tHl9L-evr19pB9_6xgC_slpL1KMgfU130_provenance
;
np:hasPublicationInfo
dgn-np:NP864893.RAopgSiYsHfUJD0tHl9L-evr19pB9_6xgC_slpL1KMgfU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP864893.RAopgSiYsHfUJD0tHl9L-evr19pB9_6xgC_slpL1KMgfU130_assertion
a
np:Assertion
.
dgn-np:NP864893.RAopgSiYsHfUJD0tHl9L-evr19pB9_6xgC_slpL1KMgfU130_provenance
a
np:Provenance
.
dgn-np:NP864893.RAopgSiYsHfUJD0tHl9L-evr19pB9_6xgC_slpL1KMgfU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP864893.RAopgSiYsHfUJD0tHl9L-evr19pB9_6xgC_slpL1KMgfU130_assertion
{
miriam-gene:10230
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNe27d697dd51b5854348ae0d6e8daec76
sio:SIO_000628
miriam-gene:10230
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP864893.RAopgSiYsHfUJD0tHl9L-evr19pB9_6xgC_slpL1KMgfU130_provenance
{
dgn-np:NP864893.RAopgSiYsHfUJD0tHl9L-evr19pB9_6xgC_slpL1KMgfU130_assertion
dcterms:description
"[Single-strand conformation polymorphism (SSCP) analysis of the NBR2 gene failed to identify any mutations in either breast or ovarian cancer, suggesting that if the NBR2 gene is involved in the development of these cancers, other mechanisms for tumorigenesis may exist.]. 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:9215675
;
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:NP864893.RAopgSiYsHfUJD0tHl9L-evr19pB9_6xgC_slpL1KMgfU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:48+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" .
}