@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60
> .
@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:NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_head
{
this:
np:hasAssertion
dgn-np:NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_assertion
;
np:hasProvenance
dgn-np:NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_provenance
;
np:hasPublicationInfo
dgn-np:NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_assertion
a
np:Assertion
.
dgn-np:NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_provenance
a
np:Provenance
.
dgn-np:NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_assertion
{
miriam-gene:2200
a
ncit:C16612
.
lld:C0009782
a
ncit:C7057
.
dgn-gda:DGN66a47bc1ee16a90c0e18cf71486799cf
sio:SIO_000628
miriam-gene:2200
,
lld:C0009782
;
a
sio:SIO_001121
.
}
dgn-np:NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_provenance
{
dgn-np:NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_assertion
dcterms:description
"[Our findings expand the number of large FBN1 deletions, and emphasize the importance of screening for large genomic deletions in connective tissue disorders featuring aortopathies, especially for those with classic Marfan phenotype.]. 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:21936929
;
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:NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:44+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" .
}