@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP406919.RA5ivaS5MXFhJc73ywWFGgqxLEjbt_sN3sg73NBygHrsU
> .
@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/v3.0.0/void/
> .
dgn-np:NP406919.RA5ivaS5MXFhJc73ywWFGgqxLEjbt_sN3sg73NBygHrsU130_head
{
this:
np:hasAssertion
dgn-np:NP406919.RA5ivaS5MXFhJc73ywWFGgqxLEjbt_sN3sg73NBygHrsU130_assertion
;
np:hasProvenance
dgn-np:NP406919.RA5ivaS5MXFhJc73ywWFGgqxLEjbt_sN3sg73NBygHrsU130_provenance
;
np:hasPublicationInfo
dgn-np:NP406919.RA5ivaS5MXFhJc73ywWFGgqxLEjbt_sN3sg73NBygHrsU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP406919.RA5ivaS5MXFhJc73ywWFGgqxLEjbt_sN3sg73NBygHrsU130_assertion
a
np:Assertion
.
dgn-np:NP406919.RA5ivaS5MXFhJc73ywWFGgqxLEjbt_sN3sg73NBygHrsU130_provenance
a
np:Provenance
.
dgn-np:NP406919.RA5ivaS5MXFhJc73ywWFGgqxLEjbt_sN3sg73NBygHrsU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP406919.RA5ivaS5MXFhJc73ywWFGgqxLEjbt_sN3sg73NBygHrsU130_assertion
{
miriam-gene:2316
a
ncit:C16612
.
lld:C0340364
a
ncit:C7057
.
dgn-gda:DGNb0bc6c6745bf1f3ee77ef75bcb3a1878
sio:SIO_000628
miriam-gene:2316
,
lld:C0340364
;
a
sio:SIO_001121
.
}
dgn-np:NP406919.RA5ivaS5MXFhJc73ywWFGgqxLEjbt_sN3sg73NBygHrsU130_provenance
{
dgn-np:NP406919.RA5ivaS5MXFhJc73ywWFGgqxLEjbt_sN3sg73NBygHrsU130_assertion
dcterms:description
"[Advances in phenotypic classification have led to linkage to sites on chromosomes 11, 13 and 16 and identification of the first mutation in familial mitral valve prolapse not related to connective tissue syndromes - an X-linked filamin A mutation.]. 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:17413272
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP406919.RA5ivaS5MXFhJc73ywWFGgqxLEjbt_sN3sg73NBygHrsU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:36+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}