@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP228260.RAGm1gTpazU1vyADZ-yxSPGC35bM_nhW_Jyvzqvc17bH0
> .
@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:NP228260.RAGm1gTpazU1vyADZ-yxSPGC35bM_nhW_Jyvzqvc17bH0130_head
{
this:
np:hasAssertion
dgn-np:NP228260.RAGm1gTpazU1vyADZ-yxSPGC35bM_nhW_Jyvzqvc17bH0130_assertion
;
np:hasProvenance
dgn-np:NP228260.RAGm1gTpazU1vyADZ-yxSPGC35bM_nhW_Jyvzqvc17bH0130_provenance
;
np:hasPublicationInfo
dgn-np:NP228260.RAGm1gTpazU1vyADZ-yxSPGC35bM_nhW_Jyvzqvc17bH0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP228260.RAGm1gTpazU1vyADZ-yxSPGC35bM_nhW_Jyvzqvc17bH0130_assertion
a
np:Assertion
.
dgn-np:NP228260.RAGm1gTpazU1vyADZ-yxSPGC35bM_nhW_Jyvzqvc17bH0130_provenance
a
np:Provenance
.
dgn-np:NP228260.RAGm1gTpazU1vyADZ-yxSPGC35bM_nhW_Jyvzqvc17bH0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP228260.RAGm1gTpazU1vyADZ-yxSPGC35bM_nhW_Jyvzqvc17bH0130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0005779
a
ncit:C7057
.
dgn-gda:DGNd205772d0d6468449f487c219dfaf837
sio:SIO_000628
miriam-gene:2147
,
lld:C0005779
;
a
sio:SIO_001121
.
}
dgn-np:NP228260.RAGm1gTpazU1vyADZ-yxSPGC35bM_nhW_Jyvzqvc17bH0130_provenance
{
dgn-np:NP228260.RAGm1gTpazU1vyADZ-yxSPGC35bM_nhW_Jyvzqvc17bH0130_assertion
dcterms:description
"[Compared with that of human prothrombin, variation at critical recognition sites would likely alter its binding affinity and reaction velocity, which would contribute to coagulation disorder when porcine liver is transplanted into human body.]. 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:17188533
;
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:NP228260.RAGm1gTpazU1vyADZ-yxSPGC35bM_nhW_Jyvzqvc17bH0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}