@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc
> .
@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:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_head
{
this:
np:hasAssertion
dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_assertion
;
np:hasProvenance
dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_provenance
;
np:hasPublicationInfo
dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_assertion
a
np:Assertion
.
dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_provenance
a
np:Provenance
.
dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_assertion
{
miriam-gene:2811
a
ncit:C16612
.
lld:C0005129
a
ncit:C7057
.
dgn-gda:DGN813b24ba5072c323b78e4aad00c15ce7
sio:SIO_000628
miriam-gene:2811
,
lld:C0005129
;
a
sio:SIO_001121
.
}
dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_provenance
{
dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_assertion
dcterms:description
"[Underlying this disorder of platelet function is a defect in the platelet glycoprotein (GP) Ib-IX-V complex, composed of four polypeptides, GP Ib alpha, GP Ib beta, GP IX, and GP V. Molecular characterization of individuals with BSs has identified mutations in the GP Ib alpha, GP Ib beta, and GP IX genes responsible for the expressed 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:10996832
;
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:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:40+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" .
}