@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP920153.RAYNlBjA-AqtsFvNvNr2L2-u2HtZfOK-JGfoDzf8U6X8o
> .
@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:NP920153.RAYNlBjA-AqtsFvNvNr2L2-u2HtZfOK-JGfoDzf8U6X8o130_head
{
this:
np:hasAssertion
dgn-np:NP920153.RAYNlBjA-AqtsFvNvNr2L2-u2HtZfOK-JGfoDzf8U6X8o130_assertion
;
np:hasProvenance
dgn-np:NP920153.RAYNlBjA-AqtsFvNvNr2L2-u2HtZfOK-JGfoDzf8U6X8o130_provenance
;
np:hasPublicationInfo
dgn-np:NP920153.RAYNlBjA-AqtsFvNvNr2L2-u2HtZfOK-JGfoDzf8U6X8o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP920153.RAYNlBjA-AqtsFvNvNr2L2-u2HtZfOK-JGfoDzf8U6X8o130_assertion
a
np:Assertion
.
dgn-np:NP920153.RAYNlBjA-AqtsFvNvNr2L2-u2HtZfOK-JGfoDzf8U6X8o130_provenance
a
np:Provenance
.
dgn-np:NP920153.RAYNlBjA-AqtsFvNvNr2L2-u2HtZfOK-JGfoDzf8U6X8o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP920153.RAYNlBjA-AqtsFvNvNr2L2-u2HtZfOK-JGfoDzf8U6X8o130_assertion
{
miriam-gene:2688
a
ncit:C16612
.
lld:C0410529
a
ncit:C7057
.
dgn-gda:DGN5e0896099c9a005e79dd9ff4fb37c45f
sio:SIO_000628
miriam-gene:2688
,
lld:C0410529
;
a
sio:SIO_001121
.
}
dgn-np:NP920153.RAYNlBjA-AqtsFvNvNr2L2-u2HtZfOK-JGfoDzf8U6X8o130_provenance
{
dgn-np:NP920153.RAYNlBjA-AqtsFvNvNr2L2-u2HtZfOK-JGfoDzf8U6X8o130_assertion
dcterms:description
"[The effects of recombinant human growth hormone (rhGH) treatment for three years were compared in patients with achondroplasia (ACH) and hypochondroplasia (HCH), whose diagnosis had been confirmed by DNA analysis of the fibroblast growth factor receptor 3 gene.]. 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:12733711
;
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:NP920153.RAYNlBjA-AqtsFvNvNr2L2-u2HtZfOK-JGfoDzf8U6X8o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:24+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" .
}