@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_assertion
a
np:Assertion
.
dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_provenance
a
np:Provenance
.
dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_assertion
{
miriam-gene:157680
a
ncit:C16612
.
lld:C0265223
a
ncit:C7057
.
dgn-gda:DGNa12ed75c7874f10f1ebe3b6ffd7168d4
sio:SIO_000628
miriam-gene:157680
,
lld:C0265223
;
a
sio:SIO_001121
.
}
dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_provenance
{
dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_assertion
dcterms:description
"[A comparison of features among different Cohen syndrome populations with shared linkage to the COH1 locus or known COH1 gene mutations may allow for the determination of improved clinical criteria on which to suspect the diagnosis of Cohen 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:15211651
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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 .
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dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:08+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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> , <
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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
}