@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP754931.RAkSfj44ofzf6wBzVZjguTS_4mNgkLl4fSB2wcLPtYpow
> .
@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:NP754931.RAkSfj44ofzf6wBzVZjguTS_4mNgkLl4fSB2wcLPtYpow130_head
{
this:
np:hasAssertion
dgn-np:NP754931.RAkSfj44ofzf6wBzVZjguTS_4mNgkLl4fSB2wcLPtYpow130_assertion
;
np:hasProvenance
dgn-np:NP754931.RAkSfj44ofzf6wBzVZjguTS_4mNgkLl4fSB2wcLPtYpow130_provenance
;
np:hasPublicationInfo
dgn-np:NP754931.RAkSfj44ofzf6wBzVZjguTS_4mNgkLl4fSB2wcLPtYpow130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP754931.RAkSfj44ofzf6wBzVZjguTS_4mNgkLl4fSB2wcLPtYpow130_assertion
a
np:Assertion
.
dgn-np:NP754931.RAkSfj44ofzf6wBzVZjguTS_4mNgkLl4fSB2wcLPtYpow130_provenance
a
np:Provenance
.
dgn-np:NP754931.RAkSfj44ofzf6wBzVZjguTS_4mNgkLl4fSB2wcLPtYpow130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP754931.RAkSfj44ofzf6wBzVZjguTS_4mNgkLl4fSB2wcLPtYpow130_assertion
{
miriam-gene:6804
a
ncit:C16612
.
lld:C0175702
a
ncit:C7057
.
dgn-gda:DGN2cfc884987c3f662c8f08c43d75a6e13
sio:SIO_000628
miriam-gene:6804
,
lld:C0175702
;
a
sio:SIO_001121
.
}
dgn-np:NP754931.RAkSfj44ofzf6wBzVZjguTS_4mNgkLl4fSB2wcLPtYpow130_provenance
{
dgn-np:NP754931.RAkSfj44ofzf6wBzVZjguTS_4mNgkLl4fSB2wcLPtYpow130_assertion
dcterms:description
"[This observation narrows the minimal region of deletion in WS and suggests that the syntaxin 1A and frizzled genes are not responsible for the major features of this developmental disorder and provides important insight into understanding the genotype-phenotype correlation in WS.]. 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:10874638
;
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:NP754931.RAkSfj44ofzf6wBzVZjguTS_4mNgkLl4fSB2wcLPtYpow130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:37+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" .
}