@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP498916.RAFgcsb8MbPhrZUg1NVscockfawgLYbjycFB540_FdFG0
> .
@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:NP498916.RAFgcsb8MbPhrZUg1NVscockfawgLYbjycFB540_FdFG0130_head
{
this:
np:hasAssertion
dgn-np:NP498916.RAFgcsb8MbPhrZUg1NVscockfawgLYbjycFB540_FdFG0130_assertion
;
np:hasProvenance
dgn-np:NP498916.RAFgcsb8MbPhrZUg1NVscockfawgLYbjycFB540_FdFG0130_provenance
;
np:hasPublicationInfo
dgn-np:NP498916.RAFgcsb8MbPhrZUg1NVscockfawgLYbjycFB540_FdFG0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP498916.RAFgcsb8MbPhrZUg1NVscockfawgLYbjycFB540_FdFG0130_assertion
a
np:Assertion
.
dgn-np:NP498916.RAFgcsb8MbPhrZUg1NVscockfawgLYbjycFB540_FdFG0130_provenance
a
np:Provenance
.
dgn-np:NP498916.RAFgcsb8MbPhrZUg1NVscockfawgLYbjycFB540_FdFG0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP498916.RAFgcsb8MbPhrZUg1NVscockfawgLYbjycFB540_FdFG0130_assertion
{
miriam-gene:2158
a
ncit:C16612
.
lld:C1839238
a
ncit:C7057
.
dgn-gda:DGN42df2fec863e7902fce7b452f03396e3
sio:SIO_000628
miriam-gene:2158
,
lld:C1839238
;
a
sio:SIO_001121
.
}
dgn-np:NP498916.RAFgcsb8MbPhrZUg1NVscockfawgLYbjycFB540_FdFG0130_provenance
{
dgn-np:NP498916.RAFgcsb8MbPhrZUg1NVscockfawgLYbjycFB540_FdFG0130_assertion
dcterms:description
"[A normal human population has been screened for the existence of further restriction fragment length polymorphisms (RFLPs) in the clotting factor IX gene in addition to the TaqI polymorphism already characterised (1,2).]. 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:6096810
;
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:NP498916.RAFgcsb8MbPhrZUg1NVscockfawgLYbjycFB540_FdFG0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:57+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" .
}