@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP597783.RAihvbc9lu7jXOX6qC0ITCLPSrS5-moY1Hr272vyx9mgA
> .
@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:NP597783.RAihvbc9lu7jXOX6qC0ITCLPSrS5-moY1Hr272vyx9mgA130_head
{
this:
np:hasAssertion
dgn-np:NP597783.RAihvbc9lu7jXOX6qC0ITCLPSrS5-moY1Hr272vyx9mgA130_assertion
;
np:hasProvenance
dgn-np:NP597783.RAihvbc9lu7jXOX6qC0ITCLPSrS5-moY1Hr272vyx9mgA130_provenance
;
np:hasPublicationInfo
dgn-np:NP597783.RAihvbc9lu7jXOX6qC0ITCLPSrS5-moY1Hr272vyx9mgA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP597783.RAihvbc9lu7jXOX6qC0ITCLPSrS5-moY1Hr272vyx9mgA130_assertion
a
np:Assertion
.
dgn-np:NP597783.RAihvbc9lu7jXOX6qC0ITCLPSrS5-moY1Hr272vyx9mgA130_provenance
a
np:Provenance
.
dgn-np:NP597783.RAihvbc9lu7jXOX6qC0ITCLPSrS5-moY1Hr272vyx9mgA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP597783.RAihvbc9lu7jXOX6qC0ITCLPSrS5-moY1Hr272vyx9mgA130_assertion
{
miriam-gene:5048
a
ncit:C16612
.
lld:C0265219
a
ncit:C7057
.
dgn-gda:DGN2fd88015e7bb01f0cfa15d43138a5835
sio:SIO_000628
miriam-gene:5048
,
lld:C0265219
;
a
sio:SIO_001121
.
}
dgn-np:NP597783.RAihvbc9lu7jXOX6qC0ITCLPSrS5-moY1Hr272vyx9mgA130_provenance
{
dgn-np:NP597783.RAihvbc9lu7jXOX6qC0ITCLPSrS5-moY1Hr272vyx9mgA130_assertion
dcterms:description
"[Our analyses also suggest that additional genes distal to LIS1 may be responsible for the facial dysmorphology and other abnormalities seen in MDS but not in ILS patients, supporting our original concept MDS as a contiguous gene deletion syndrome.]. 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:9063734
;
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:NP597783.RAihvbc9lu7jXOX6qC0ITCLPSrS5-moY1Hr272vyx9mgA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:59+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" .
}