@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc
> .
@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:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_head
{
this:
np:hasAssertion
dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_assertion
;
np:hasProvenance
dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_provenance
;
np:hasPublicationInfo
dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_assertion
a
np:Assertion
.
dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_provenance
a
np:Provenance
.
dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_assertion
{
miriam-gene:2335
a
ncit:C16612
.
lld:C0086437
a
ncit:C7057
.
dgn-gda:DGN709e2c95035e4ed7ed0914b2fb0eff4b
sio:SIO_000628
miriam-gene:2335
,
lld:C0086437
;
a
sio:SIO_001121
.
}
dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_provenance
{
dgn-np:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_assertion
dcterms:description
"[Since fibronectin is an important adhesive glycoprotein in connective tissue and is required for normal platelet interactions with collagen, we propose that both platelet malfunction and joint hypermobility in this kindred are likely explained by a defective fibronectin.]. 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:7382073
;
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:NP228902.RABKBH3Sjj3gC_1mXDSgTh4DnIqkKqPm4Ve_eP90gn4lc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}