@prefix orcid: . @prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP254081.RAhBQaIozngrkah5aJ-lb_TPlXPW5jsfgKZ4osu29NHOs130_head { this: np:hasAssertion dgn-np:NP254081.RAhBQaIozngrkah5aJ-lb_TPlXPW5jsfgKZ4osu29NHOs130_assertion; np:hasProvenance dgn-np:NP254081.RAhBQaIozngrkah5aJ-lb_TPlXPW5jsfgKZ4osu29NHOs130_provenance; np:hasPublicationInfo dgn-np:NP254081.RAhBQaIozngrkah5aJ-lb_TPlXPW5jsfgKZ4osu29NHOs130_publicationInfo; a np:Nanopublication . dgn-np:NP254081.RAhBQaIozngrkah5aJ-lb_TPlXPW5jsfgKZ4osu29NHOs130_assertion a np:Assertion . dgn-np:NP254081.RAhBQaIozngrkah5aJ-lb_TPlXPW5jsfgKZ4osu29NHOs130_provenance a np:Provenance . dgn-np:NP254081.RAhBQaIozngrkah5aJ-lb_TPlXPW5jsfgKZ4osu29NHOs130_publicationInfo a np:PublicationInfo . } dgn-np:NP254081.RAhBQaIozngrkah5aJ-lb_TPlXPW5jsfgKZ4osu29NHOs130_assertion { miriam-gene:444 a ncit:C16612 . lld:C1266034 a ncit:C7057 . dgn-gda:DGNa7b39c05f0db4faf7d60fc6a694be078 sio:SIO_000628 miriam-gene:444, lld:C1266034; a sio:SIO_001121 . } dgn-np:NP254081.RAhBQaIozngrkah5aJ-lb_TPlXPW5jsfgKZ4osu29NHOs130_provenance { dgn-np:NP254081.RAhBQaIozngrkah5aJ-lb_TPlXPW5jsfgKZ4osu29NHOs130_assertion dcterms:description "[In this study, we examined EGFR and KRAS gene mutations in 119 synchronous pulmonary lesions, including 40 precursor lesions (atypical adenomatous hyperplasia, AAH), 26 carcinomas in situ (non-mucinous bronchioloalveolar carcinoma, BAC), 14 minimally invasive adenocarcinomas, 34 overt invasive adenocarcinomas, and five of other subtypes of cancer.]. 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:17534846; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP254081.RAhBQaIozngrkah5aJ-lb_TPlXPW5jsfgKZ4osu29NHOs130_publicationInfo { this: dcterms:created "2015-08-25T14:40:04+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X, orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654; pav:createdBy orcid:0000-0003-0169-8159; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }