@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP308441.RAUe9w50WOMKy8s2G6I6b5kAfI1c7Y9gwhB2BYFZvXYFY
> .
@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:NP308441.RAUe9w50WOMKy8s2G6I6b5kAfI1c7Y9gwhB2BYFZvXYFY130_head
{
this:
np:hasAssertion
dgn-np:NP308441.RAUe9w50WOMKy8s2G6I6b5kAfI1c7Y9gwhB2BYFZvXYFY130_assertion
;
np:hasProvenance
dgn-np:NP308441.RAUe9w50WOMKy8s2G6I6b5kAfI1c7Y9gwhB2BYFZvXYFY130_provenance
;
np:hasPublicationInfo
dgn-np:NP308441.RAUe9w50WOMKy8s2G6I6b5kAfI1c7Y9gwhB2BYFZvXYFY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP308441.RAUe9w50WOMKy8s2G6I6b5kAfI1c7Y9gwhB2BYFZvXYFY130_assertion
a
np:Assertion
.
dgn-np:NP308441.RAUe9w50WOMKy8s2G6I6b5kAfI1c7Y9gwhB2BYFZvXYFY130_provenance
a
np:Provenance
.
dgn-np:NP308441.RAUe9w50WOMKy8s2G6I6b5kAfI1c7Y9gwhB2BYFZvXYFY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP308441.RAUe9w50WOMKy8s2G6I6b5kAfI1c7Y9gwhB2BYFZvXYFY130_assertion
{
miriam-gene:9232
a
ncit:C16612
.
lld:C0032019
a
ncit:C7057
.
dgn-gda:DGN12f8c401814fcce291ede789ed44590d
sio:SIO_000628
miriam-gene:9232
,
lld:C0032019
;
a
sio:SIO_001121
.
}
dgn-np:NP308441.RAUe9w50WOMKy8s2G6I6b5kAfI1c7Y9gwhB2BYFZvXYFY130_provenance
{
dgn-np:NP308441.RAUe9w50WOMKy8s2G6I6b5kAfI1c7Y9gwhB2BYFZvXYFY130_assertion
dcterms:description
"[The human PTTG family consists of at least three homologous genes, of which PTTG1 is located on chromosome 5q33 and is expressed at low levels in most normal human tissues but is highly expressed in malignant human cell lines and in pituitary tumors.]. 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:10546001
;
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:NP308441.RAUe9w50WOMKy8s2G6I6b5kAfI1c7Y9gwhB2BYFZvXYFY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:57+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" .
}