@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP641366.RAZCZv_ohcJfqLRSX1tr6-F-xADQEvAQimZxjL2gbcFAw
> .
@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:NP641366.RAZCZv_ohcJfqLRSX1tr6-F-xADQEvAQimZxjL2gbcFAw130_head
{
this:
np:hasAssertion
dgn-np:NP641366.RAZCZv_ohcJfqLRSX1tr6-F-xADQEvAQimZxjL2gbcFAw130_assertion
;
np:hasProvenance
dgn-np:NP641366.RAZCZv_ohcJfqLRSX1tr6-F-xADQEvAQimZxjL2gbcFAw130_provenance
;
np:hasPublicationInfo
dgn-np:NP641366.RAZCZv_ohcJfqLRSX1tr6-F-xADQEvAQimZxjL2gbcFAw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP641366.RAZCZv_ohcJfqLRSX1tr6-F-xADQEvAQimZxjL2gbcFAw130_assertion
a
np:Assertion
.
dgn-np:NP641366.RAZCZv_ohcJfqLRSX1tr6-F-xADQEvAQimZxjL2gbcFAw130_provenance
a
np:Provenance
.
dgn-np:NP641366.RAZCZv_ohcJfqLRSX1tr6-F-xADQEvAQimZxjL2gbcFAw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP641366.RAZCZv_ohcJfqLRSX1tr6-F-xADQEvAQimZxjL2gbcFAw130_assertion
{
miriam-gene:462
a
ncit:C16612
.
lld:C0040046
a
ncit:C7057
.
dgn-gda:DGN3d0f110fd120e036d4ca83b00222afa9
sio:SIO_000628
miriam-gene:462
,
lld:C0040046
;
a
sio:SIO_001121
.
}
dgn-np:NP641366.RAZCZv_ohcJfqLRSX1tr6-F-xADQEvAQimZxjL2gbcFAw130_provenance
{
dgn-np:NP641366.RAZCZv_ohcJfqLRSX1tr6-F-xADQEvAQimZxjL2gbcFAw130_assertion
dcterms:description
"[Structural analyses of a hereditary abnormal antithrombin III, antithrombin III Toyama, which has normal progressive antithrombin activity but no heparin cofactor activity, have been carried out to elucidate the molecular abnormality causing recurrent thrombophlebitis of a patient and to identify an amino acid residue essential for the binding with heparin.]. 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:6582486
;
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:NP641366.RAZCZv_ohcJfqLRSX1tr6-F-xADQEvAQimZxjL2gbcFAw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:26+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" .
}