@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP157772.RAUDFThuF-fZVU6JFyBAdNGDoyDgZf82zXCMJ00rn0uXk
> .
@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:NP157772.RAUDFThuF-fZVU6JFyBAdNGDoyDgZf82zXCMJ00rn0uXk130_head
{
this:
np:hasAssertion
dgn-np:NP157772.RAUDFThuF-fZVU6JFyBAdNGDoyDgZf82zXCMJ00rn0uXk130_assertion
;
np:hasProvenance
dgn-np:NP157772.RAUDFThuF-fZVU6JFyBAdNGDoyDgZf82zXCMJ00rn0uXk130_provenance
;
np:hasPublicationInfo
dgn-np:NP157772.RAUDFThuF-fZVU6JFyBAdNGDoyDgZf82zXCMJ00rn0uXk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP157772.RAUDFThuF-fZVU6JFyBAdNGDoyDgZf82zXCMJ00rn0uXk130_assertion
a
np:Assertion
.
dgn-np:NP157772.RAUDFThuF-fZVU6JFyBAdNGDoyDgZf82zXCMJ00rn0uXk130_provenance
a
np:Provenance
.
dgn-np:NP157772.RAUDFThuF-fZVU6JFyBAdNGDoyDgZf82zXCMJ00rn0uXk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP157772.RAUDFThuF-fZVU6JFyBAdNGDoyDgZf82zXCMJ00rn0uXk130_assertion
{
miriam-gene:2694
a
ncit:C16612
.
lld:C0002888
a
ncit:C7057
.
dgn-gda:DGN341db9b8cbbd974df23ac797c132a2ab
sio:SIO_000628
miriam-gene:2694
,
lld:C0002888
;
a
sio:SIO_001121
.
}
dgn-np:NP157772.RAUDFThuF-fZVU6JFyBAdNGDoyDgZf82zXCMJ00rn0uXk130_provenance
{
dgn-np:NP157772.RAUDFThuF-fZVU6JFyBAdNGDoyDgZf82zXCMJ00rn0uXk130_assertion
dcterms:description
"[Several syndromes present with megaloblastic anemia such as congenital megaloblastic anemia due to intrinsic factor defect and juvenile megaloblastic anemia with proteinuria due to defects in the cubilin or the amnionless protein.]. 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:16047053
;
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:NP157772.RAUDFThuF-fZVU6JFyBAdNGDoyDgZf82zXCMJ00rn0uXk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:25+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" .
}