@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP482954.RAznLms1zWFkNq2sYVQob7S-HgmUKYqFL5z9za4BGULMc
> .
@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:NP482954.RAznLms1zWFkNq2sYVQob7S-HgmUKYqFL5z9za4BGULMc130_head
{
this:
np:hasAssertion
dgn-np:NP482954.RAznLms1zWFkNq2sYVQob7S-HgmUKYqFL5z9za4BGULMc130_assertion
;
np:hasProvenance
dgn-np:NP482954.RAznLms1zWFkNq2sYVQob7S-HgmUKYqFL5z9za4BGULMc130_provenance
;
np:hasPublicationInfo
dgn-np:NP482954.RAznLms1zWFkNq2sYVQob7S-HgmUKYqFL5z9za4BGULMc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP482954.RAznLms1zWFkNq2sYVQob7S-HgmUKYqFL5z9za4BGULMc130_assertion
a
np:Assertion
.
dgn-np:NP482954.RAznLms1zWFkNq2sYVQob7S-HgmUKYqFL5z9za4BGULMc130_provenance
a
np:Provenance
.
dgn-np:NP482954.RAznLms1zWFkNq2sYVQob7S-HgmUKYqFL5z9za4BGULMc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP482954.RAznLms1zWFkNq2sYVQob7S-HgmUKYqFL5z9za4BGULMc130_assertion
{
miriam-gene:2691
a
ncit:C16612
.
lld:C0001206
a
ncit:C7057
.
dgn-gda:DGNca7e657f7eb3316acd139d3075b519e4
sio:SIO_000628
miriam-gene:2691
,
lld:C0001206
;
a
sio:SIO_001121
.
}
dgn-np:NP482954.RAznLms1zWFkNq2sYVQob7S-HgmUKYqFL5z9za4BGULMc130_provenance
{
dgn-np:NP482954.RAznLms1zWFkNq2sYVQob7S-HgmUKYqFL5z9za4BGULMc130_assertion
dcterms:description
"[GHRH observed in acromegalic and normal subjects, it is unlikely that subjects possessing the rarer form containing Thr in place of Ala at residue 57 are at increased risk of developing acromegaly.]. 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:12220735
;
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:NP482954.RAznLms1zWFkNq2sYVQob7S-HgmUKYqFL5z9za4BGULMc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:49+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" .
}