@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_head
{
this:
np:hasAssertion
dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_assertion
;
np:hasProvenance
dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_provenance
;
np:hasPublicationInfo
dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_assertion
a
np:Assertion
.
dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_provenance
a
np:Provenance
.
dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C0587248
a
ncit:C7057
.
dgn-gda:DGN5e03417ee6240bab2fdd06a7f919f100
sio:SIO_000628
miriam-gene:3845
,
lld:C0587248
;
a
sio:SIO_001121
.
}
dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_provenance
{
dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_assertion
dcterms:description
"[In conclusion, our data underscore the important role of RAS in the pathogenesis of the group of related disorders including NS, CFCS, and CS, and provide clues to the high phenotypic variability of patients with germline KRAS mutations.]. 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:20949621
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:08+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}