@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms
> .
@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:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_head
{
this:
np:hasAssertion
dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_assertion
;
np:hasProvenance
dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_provenance
;
np:hasPublicationInfo
dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_assertion
a
np:Assertion
.
dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_provenance
a
np:Provenance
.
dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_assertion
{
miriam-gene:5554
a
ncit:C16612
.
lld:C0008533
a
ncit:C7057
.
dgn-gda:DGNbbf11fc638d2f80d82cd31bf72d2c2ba
sio:SIO_000628
miriam-gene:5554
,
lld:C0008533
;
a
sio:SIO_001121
.
}
dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_provenance
{
dgn-np:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_assertion
dcterms:description
"[The likelihood of a missense mutation causing hemophilia B depends on whether the residue is also conserved in the factor IX-related proteases: factor VII, factor X, and protein C. Most of the possible missense mutations in generically conserved residues (i.e., those conserved in factor IX and in all the related proteases) should cause disease.]. 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:1680287
;
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:NP939873.RA4kTEBBOCAshRyCXhP0ZAQJE2jwebX8kbuLxZ_2OCDms130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:36+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" .
}