@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4
> .
@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:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_head
{
this:
np:hasAssertion
dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_assertion
;
np:hasProvenance
dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_provenance
;
np:hasPublicationInfo
dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_assertion
a
np:Assertion
.
dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_provenance
a
np:Provenance
.
dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_assertion
{
miriam-gene:3716
a
ncit:C16612
.
lld:C0085669
a
ncit:C7057
.
dgn-gda:DGNd9efe629d53d4b475773fa40a90fc920
sio:SIO_000628
miriam-gene:3716
,
lld:C0085669
;
a
sio:SIO_001121
.
}
dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_provenance
{
dgn-np:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_assertion
dcterms:description
"[Although we isolated a mutation of JAK1 at residue Val658, which is found mutated in acute leukaemia patients, most of the mutations we identified are within the kinase domain and have yet to be identified in patients.]. 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:20868368
;
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:NP795680.RA3Vk3LsVB7mmKvdyBiTxPLYLhpEZKu3CAGNeHCUVVNy4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:08+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" .
}