@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP742047.RAbe0wCB0ALypt9UwESYKciRNSOb1yiaz8ZMK5sjyiU_E
> .
@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:NP742047.RAbe0wCB0ALypt9UwESYKciRNSOb1yiaz8ZMK5sjyiU_E130_head
{
this:
np:hasAssertion
dgn-np:NP742047.RAbe0wCB0ALypt9UwESYKciRNSOb1yiaz8ZMK5sjyiU_E130_assertion
;
np:hasProvenance
dgn-np:NP742047.RAbe0wCB0ALypt9UwESYKciRNSOb1yiaz8ZMK5sjyiU_E130_provenance
;
np:hasPublicationInfo
dgn-np:NP742047.RAbe0wCB0ALypt9UwESYKciRNSOb1yiaz8ZMK5sjyiU_E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP742047.RAbe0wCB0ALypt9UwESYKciRNSOb1yiaz8ZMK5sjyiU_E130_assertion
a
np:Assertion
.
dgn-np:NP742047.RAbe0wCB0ALypt9UwESYKciRNSOb1yiaz8ZMK5sjyiU_E130_provenance
a
np:Provenance
.
dgn-np:NP742047.RAbe0wCB0ALypt9UwESYKciRNSOb1yiaz8ZMK5sjyiU_E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP742047.RAbe0wCB0ALypt9UwESYKciRNSOb1yiaz8ZMK5sjyiU_E130_assertion
{
miriam-gene:3479
a
ncit:C16612
.
lld:C0025958
a
ncit:C7057
.
dgn-gda:DGNe9286446e13f6e84063afabe16f23ec8
sio:SIO_000628
miriam-gene:3479
,
lld:C0025958
;
a
sio:SIO_001121
.
}
dgn-np:NP742047.RAbe0wCB0ALypt9UwESYKciRNSOb1yiaz8ZMK5sjyiU_E130_provenance
{
dgn-np:NP742047.RAbe0wCB0ALypt9UwESYKciRNSOb1yiaz8ZMK5sjyiU_E130_assertion
dcterms:description
"[The importance of IGF-I for both in utero as well as postnatal human growth is highlighted by rare human homozygous IGF1 mutations, which are characterized by intrauterine growth retardation (IUGR), microcephaly, mental retardation and severe postnatal growth failure.]. 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:23502138
;
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:NP742047.RAbe0wCB0ALypt9UwESYKciRNSOb1yiaz8ZMK5sjyiU_E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:30+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" .
}