@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP662082.RAHzC_6CvxH_T_snxYtBzkt5PK60A3zAmwk0M0SBUDYjM
> .
@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:NP662082.RAHzC_6CvxH_T_snxYtBzkt5PK60A3zAmwk0M0SBUDYjM130_head
{
this:
np:hasAssertion
dgn-np:NP662082.RAHzC_6CvxH_T_snxYtBzkt5PK60A3zAmwk0M0SBUDYjM130_assertion
;
np:hasProvenance
dgn-np:NP662082.RAHzC_6CvxH_T_snxYtBzkt5PK60A3zAmwk0M0SBUDYjM130_provenance
;
np:hasPublicationInfo
dgn-np:NP662082.RAHzC_6CvxH_T_snxYtBzkt5PK60A3zAmwk0M0SBUDYjM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP662082.RAHzC_6CvxH_T_snxYtBzkt5PK60A3zAmwk0M0SBUDYjM130_assertion
a
np:Assertion
.
dgn-np:NP662082.RAHzC_6CvxH_T_snxYtBzkt5PK60A3zAmwk0M0SBUDYjM130_provenance
a
np:Provenance
.
dgn-np:NP662082.RAHzC_6CvxH_T_snxYtBzkt5PK60A3zAmwk0M0SBUDYjM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP662082.RAHzC_6CvxH_T_snxYtBzkt5PK60A3zAmwk0M0SBUDYjM130_assertion
{
miriam-gene:3161
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNe7fb302b03654c12eb1e88027e1c0ada
sio:SIO_000628
miriam-gene:3161
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP662082.RAHzC_6CvxH_T_snxYtBzkt5PK60A3zAmwk0M0SBUDYjM130_provenance
{
dgn-np:NP662082.RAHzC_6CvxH_T_snxYtBzkt5PK60A3zAmwk0M0SBUDYjM130_assertion
dcterms:description
"[For the triple axis of HA, HAS1 and RHAMM, mutations in HAS1 provide an indicator that these aberrations contribute to the events that lead to malignancy through increased risk and predisposition.]. 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:23517594
;
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:NP662082.RAHzC_6CvxH_T_snxYtBzkt5PK60A3zAmwk0M0SBUDYjM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:40+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" .
}