@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg
> .
@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:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_head
{
this:
np:hasAssertion
dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_assertion
;
np:hasProvenance
dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_provenance
;
np:hasPublicationInfo
dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_assertion
a
np:Assertion
.
dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_provenance
a
np:Provenance
.
dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_assertion
{
miriam-gene:147495
a
ncit:C16612
.
lld:C0030312
a
ncit:C7057
.
dgn-gda:DGNb8c91b6a73e3540eb10a62cf25a8ff91
sio:SIO_000628
miriam-gene:147495
,
lld:C0030312
;
a
sio:SIO_001121
.
}
dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_provenance
{
dgn-np:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_assertion
dcterms:description
"[In addition to the previously described important signs of HHS, i.e., prenatal growth retardation, microcephaly, psychomotor retardation, progressive pancytopenia, immunological abnormalities, and cerebellar hypoplasia and ataxia, we consider that delayed myelination of cerebral white matter and hypoplastic corpus callosum should be added to the list of important signs.]. 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:10963101
;
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:NP527008.RAmWkKevoi0OZDSxyvwwuhJrIJslTYj2mQchaVT6gm3dg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:16+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" .
}