@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP269945.RANTYhk-tsj01Pgc6Cd_R0ke-c0DrHaL80IGJRjn2NX-I
> .
@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:NP269945.RANTYhk-tsj01Pgc6Cd_R0ke-c0DrHaL80IGJRjn2NX-I130_head
{
this:
np:hasAssertion
dgn-np:NP269945.RANTYhk-tsj01Pgc6Cd_R0ke-c0DrHaL80IGJRjn2NX-I130_assertion
;
np:hasProvenance
dgn-np:NP269945.RANTYhk-tsj01Pgc6Cd_R0ke-c0DrHaL80IGJRjn2NX-I130_provenance
;
np:hasPublicationInfo
dgn-np:NP269945.RANTYhk-tsj01Pgc6Cd_R0ke-c0DrHaL80IGJRjn2NX-I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP269945.RANTYhk-tsj01Pgc6Cd_R0ke-c0DrHaL80IGJRjn2NX-I130_assertion
a
np:Assertion
.
dgn-np:NP269945.RANTYhk-tsj01Pgc6Cd_R0ke-c0DrHaL80IGJRjn2NX-I130_provenance
a
np:Provenance
.
dgn-np:NP269945.RANTYhk-tsj01Pgc6Cd_R0ke-c0DrHaL80IGJRjn2NX-I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP269945.RANTYhk-tsj01Pgc6Cd_R0ke-c0DrHaL80IGJRjn2NX-I130_assertion
{
miriam-gene:1351
a
ncit:C16612
.
lld:C0684275
a
ncit:C7057
.
dgn-gda:DGN034225b2806275d01e12b9c5971a270e
sio:SIO_000628
miriam-gene:1351
,
lld:C0684275
;
a
sio:SIO_001121
.
}
dgn-np:NP269945.RANTYhk-tsj01Pgc6Cd_R0ke-c0DrHaL80IGJRjn2NX-I130_provenance
{
dgn-np:NP269945.RANTYhk-tsj01Pgc6Cd_R0ke-c0DrHaL80IGJRjn2NX-I130_assertion
dcterms:description
"[Individuals with blood group A, B, AB had significantly higher levels of factor VIII related antigen (EIA) and (RIA), and ristocetin cofactor, compared with blood group O. Obligate carriers with severe haemophilia A in their families had more bleeding symptoms than corresponding group with moderate haemophilia.]. 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:6803389
;
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:NP269945.RANTYhk-tsj01Pgc6Cd_R0ke-c0DrHaL80IGJRjn2NX-I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:30+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" .
}