@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA
> .
@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:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_head
{
this:
np:hasAssertion
dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_assertion
;
np:hasProvenance
dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_provenance
;
np:hasPublicationInfo
dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_assertion
a
np:Assertion
.
dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_provenance
a
np:Provenance
.
dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_assertion
{
miriam-gene:5449
a
ncit:C16612
.
lld:C0599750
a
ncit:C7057
.
dgn-gda:DGNa6fd43e480c0b88f4088041eddf4dd87
sio:SIO_000628
miriam-gene:5449
,
lld:C0599750
;
a
sio:SIO_001121
.
}
dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_provenance
{
dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_assertion
dcterms:description
"[Mutations in Prophet of PIT1 (Prop1), one of several homeodomain transcription factors that are required for the development of the anterior pituitary gland, are the predominant cause of MPHD (multiple pituitary hormone deficiency) in humans.]. 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:15459176
;
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:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:43+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" .
}