@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP172469.RA_FzmkfKU0XLb9v9CXM2kYNt3H-Q3gFaLHC6qiBSa4xc
> .
@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:NP172469.RA_FzmkfKU0XLb9v9CXM2kYNt3H-Q3gFaLHC6qiBSa4xc130_head
{
this:
np:hasAssertion
dgn-np:NP172469.RA_FzmkfKU0XLb9v9CXM2kYNt3H-Q3gFaLHC6qiBSa4xc130_assertion
;
np:hasProvenance
dgn-np:NP172469.RA_FzmkfKU0XLb9v9CXM2kYNt3H-Q3gFaLHC6qiBSa4xc130_provenance
;
np:hasPublicationInfo
dgn-np:NP172469.RA_FzmkfKU0XLb9v9CXM2kYNt3H-Q3gFaLHC6qiBSa4xc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP172469.RA_FzmkfKU0XLb9v9CXM2kYNt3H-Q3gFaLHC6qiBSa4xc130_assertion
a
np:Assertion
.
dgn-np:NP172469.RA_FzmkfKU0XLb9v9CXM2kYNt3H-Q3gFaLHC6qiBSa4xc130_provenance
a
np:Provenance
.
dgn-np:NP172469.RA_FzmkfKU0XLb9v9CXM2kYNt3H-Q3gFaLHC6qiBSa4xc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP172469.RA_FzmkfKU0XLb9v9CXM2kYNt3H-Q3gFaLHC6qiBSa4xc130_assertion
{
miriam-gene:50947
a
ncit:C16612
.
lld:C0346010
a
ncit:C7057
.
dgn-gda:DGN2a799b940ba4fee041cfb89b89ee45a6
sio:SIO_000628
miriam-gene:50947
,
lld:C0346010
;
a
sio:SIO_001121
.
}
dgn-np:NP172469.RA_FzmkfKU0XLb9v9CXM2kYNt3H-Q3gFaLHC6qiBSa4xc130_provenance
{
dgn-np:NP172469.RA_FzmkfKU0XLb9v9CXM2kYNt3H-Q3gFaLHC6qiBSa4xc130_assertion
dcterms:description
"[As a first step toward understanding the function of BHD in the cell and how BHD mutations can lead to the BHD phenotype, we measured the expression of BHD mRNA in normal and neoplastic human tissues by fluorescent in situ hybridization.]. 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:15143337
;
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:NP172469.RA_FzmkfKU0XLb9v9CXM2kYNt3H-Q3gFaLHC6qiBSa4xc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:33+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" .
}