@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP267847.RA-EWtKR4zsSf2uG3aJxQBgtrn0rj7W_MGeGyIdlGn2Hs
> .
@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:NP267847.RA-EWtKR4zsSf2uG3aJxQBgtrn0rj7W_MGeGyIdlGn2Hs130_head
{
this:
np:hasAssertion
dgn-np:NP267847.RA-EWtKR4zsSf2uG3aJxQBgtrn0rj7W_MGeGyIdlGn2Hs130_assertion
;
np:hasProvenance
dgn-np:NP267847.RA-EWtKR4zsSf2uG3aJxQBgtrn0rj7W_MGeGyIdlGn2Hs130_provenance
;
np:hasPublicationInfo
dgn-np:NP267847.RA-EWtKR4zsSf2uG3aJxQBgtrn0rj7W_MGeGyIdlGn2Hs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP267847.RA-EWtKR4zsSf2uG3aJxQBgtrn0rj7W_MGeGyIdlGn2Hs130_assertion
a
np:Assertion
.
dgn-np:NP267847.RA-EWtKR4zsSf2uG3aJxQBgtrn0rj7W_MGeGyIdlGn2Hs130_provenance
a
np:Provenance
.
dgn-np:NP267847.RA-EWtKR4zsSf2uG3aJxQBgtrn0rj7W_MGeGyIdlGn2Hs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP267847.RA-EWtKR4zsSf2uG3aJxQBgtrn0rj7W_MGeGyIdlGn2Hs130_assertion
{
miriam-gene:867
a
ncit:C16612
.
lld:C0795841
a
ncit:C7057
.
dgn-gda:DGN74e68f4a29fd7d4b5801f72a41f5be22
sio:SIO_000628
miriam-gene:867
,
lld:C0795841
;
a
sio:SIO_001121
.
}
dgn-np:NP267847.RA-EWtKR4zsSf2uG3aJxQBgtrn0rj7W_MGeGyIdlGn2Hs130_provenance
{
dgn-np:NP267847.RA-EWtKR4zsSf2uG3aJxQBgtrn0rj7W_MGeGyIdlGn2Hs130_assertion
dcterms:description
"[The mother and brother of the reported Jacobsen syndrome child are FRA11B carriers, suggesting that in vivo breakage at the fragile site during early development could have given rise to the chromosome deletion.]. 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:7881408
;
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:NP267847.RA-EWtKR4zsSf2uG3aJxQBgtrn0rj7W_MGeGyIdlGn2Hs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:29+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" .
}