@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70
> .
@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:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_head
{
this:
np:hasAssertion
dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_assertion
;
np:hasProvenance
dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_provenance
;
np:hasPublicationInfo
dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_assertion
a
np:Assertion
.
dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_provenance
a
np:Provenance
.
dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_assertion
{
miriam-gene:1351
a
ncit:C16612
.
lld:C0005779
a
ncit:C7057
.
dgn-gda:DGNed1a611057d0b35244ab4cbb44205309
sio:SIO_000628
miriam-gene:1351
,
lld:C0005779
;
a
sio:SIO_001121
.
}
dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_provenance
{
dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_assertion
dcterms:description
"[Deficiencies of coagulation factors other than factor VIII and factor IX that cause bleeding disorders are inherited as autosomal recessive traits and are rare, with prevalences in the general population varying between 1 in 500 000 and 1 in 2 million for the homozygous forms.]. 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:15138162
;
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:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:06+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" .
}