@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP672531.RAKlb5g2xDtmMR3pKfmvdImpgjn5dmPds0b0SaA9dPa7c
> .
@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:NP672531.RAKlb5g2xDtmMR3pKfmvdImpgjn5dmPds0b0SaA9dPa7c130_head
{
this:
np:hasAssertion
dgn-np:NP672531.RAKlb5g2xDtmMR3pKfmvdImpgjn5dmPds0b0SaA9dPa7c130_assertion
;
np:hasProvenance
dgn-np:NP672531.RAKlb5g2xDtmMR3pKfmvdImpgjn5dmPds0b0SaA9dPa7c130_provenance
;
np:hasPublicationInfo
dgn-np:NP672531.RAKlb5g2xDtmMR3pKfmvdImpgjn5dmPds0b0SaA9dPa7c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP672531.RAKlb5g2xDtmMR3pKfmvdImpgjn5dmPds0b0SaA9dPa7c130_assertion
a
np:Assertion
.
dgn-np:NP672531.RAKlb5g2xDtmMR3pKfmvdImpgjn5dmPds0b0SaA9dPa7c130_provenance
a
np:Provenance
.
dgn-np:NP672531.RAKlb5g2xDtmMR3pKfmvdImpgjn5dmPds0b0SaA9dPa7c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP672531.RAKlb5g2xDtmMR3pKfmvdImpgjn5dmPds0b0SaA9dPa7c130_assertion
{
miriam-gene:2335
a
ncit:C16612
.
lld:C0013720
a
ncit:C7057
.
dgn-gda:DGNa93118621d858f0acb8930a2d4985b90
sio:SIO_000628
miriam-gene:2335
,
lld:C0013720
;
a
sio:SIO_001121
.
}
dgn-np:NP672531.RAKlb5g2xDtmMR3pKfmvdImpgjn5dmPds0b0SaA9dPa7c130_provenance
{
dgn-np:NP672531.RAKlb5g2xDtmMR3pKfmvdImpgjn5dmPds0b0SaA9dPa7c130_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-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:NP672531.RAKlb5g2xDtmMR3pKfmvdImpgjn5dmPds0b0SaA9dPa7c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:46+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" .
}