@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP249765.RAMiqD5lROZtR5shblhhGhxi4hITulQfZP6UJVmWhQeXE
> .
@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:NP249765.RAMiqD5lROZtR5shblhhGhxi4hITulQfZP6UJVmWhQeXE130_head
{
this:
np:hasAssertion
dgn-np:NP249765.RAMiqD5lROZtR5shblhhGhxi4hITulQfZP6UJVmWhQeXE130_assertion
;
np:hasProvenance
dgn-np:NP249765.RAMiqD5lROZtR5shblhhGhxi4hITulQfZP6UJVmWhQeXE130_provenance
;
np:hasPublicationInfo
dgn-np:NP249765.RAMiqD5lROZtR5shblhhGhxi4hITulQfZP6UJVmWhQeXE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP249765.RAMiqD5lROZtR5shblhhGhxi4hITulQfZP6UJVmWhQeXE130_assertion
a
np:Assertion
.
dgn-np:NP249765.RAMiqD5lROZtR5shblhhGhxi4hITulQfZP6UJVmWhQeXE130_provenance
a
np:Provenance
.
dgn-np:NP249765.RAMiqD5lROZtR5shblhhGhxi4hITulQfZP6UJVmWhQeXE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP249765.RAMiqD5lROZtR5shblhhGhxi4hITulQfZP6UJVmWhQeXE130_assertion
{
miriam-gene:5592
a
ncit:C16612
.
lld:C1704273
a
ncit:C7057
.
dgn-gda:DGN8413a44a99de9b13c6fb304ff53b1f35
sio:SIO_000628
miriam-gene:5592
,
lld:C1704273
;
a
sio:SIO_001121
.
}
dgn-np:NP249765.RAMiqD5lROZtR5shblhhGhxi4hITulQfZP6UJVmWhQeXE130_provenance
{
dgn-np:NP249765.RAMiqD5lROZtR5shblhhGhxi4hITulQfZP6UJVmWhQeXE130_assertion
dcterms:description
"[When DNA samples obtained from four widely separated sites of an adenoma were independently analyzed, each sample was found to be monoclonal and, in addition, the same allele of PGK gene was inactivated.]. 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:7910112
;
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:NP249765.RAMiqD5lROZtR5shblhhGhxi4hITulQfZP6UJVmWhQeXE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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" .
}