@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40
> .
@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:NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_head
{
this:
np:hasAssertion
dgn-np:NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_assertion
;
np:hasProvenance
dgn-np:NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_provenance
;
np:hasPublicationInfo
dgn-np:NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_assertion
a
np:Assertion
.
dgn-np:NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_provenance
a
np:Provenance
.
dgn-np:NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_assertion
{
miriam-gene:2200
a
ncit:C16612
.
lld:C0024796
a
ncit:C7057
.
dgn-gda:DGN443c23595bbd4fcb4594a9ff88983bfb
sio:SIO_000628
miriam-gene:2200
,
lld:C0024796
;
a
sio:SIO_001121
.
}
dgn-np:NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_provenance
{
dgn-np:NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_assertion
dcterms:description
"[There is a remarkable degree of clinical variability both within and between families with Marfan syndrome as well as in individuals with related disorders of connective tissue caused by FBN1 mutations and collectively termed type-1 fibrillinopathies.]. 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:11175294
;
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:NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:05+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" .
}