@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY
> .
@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/
> .
dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_head
{
this:
np:hasAssertion
dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_assertion
;
np:hasProvenance
dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_provenance
;
np:hasPublicationInfo
dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_assertion
a
np:Assertion
.
dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_provenance
a
np:Provenance
.
dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_assertion
{
miriam-gene:2335
a
ncit:C16612
.
lld:C0013720
a
ncit:C7057
.
dgn-gda:DGN557c470c4d6777d7256b9a242037f889
sio:SIO_000628
miriam-gene:2335
,
lld:C0013720
;
a
sio:SIO_001122
.
}
dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_provenance
{
dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_assertion
dcterms:description
"[Three point mutations in TNX gene were found to be associated with hypermobility type EDS and one of such mutations is the V1195M mutation at the 7th fibronectin Type III domain (TNXfn7).]. 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:20853426
;
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 .
}
dgn-np:NP840264.RAg4sP5JcDaB44PmFPgtWNZaIba-b0kD6LWBYOni3xoFY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:05+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}