@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:NP335093.RA-FSlnw04nALJD_z_04HRQpf4jH3y6xGio9E2Bnmd1Vs130_head { this: np:hasAssertion dgn-np:NP335093.RA-FSlnw04nALJD_z_04HRQpf4jH3y6xGio9E2Bnmd1Vs130_assertion; np:hasProvenance dgn-np:NP335093.RA-FSlnw04nALJD_z_04HRQpf4jH3y6xGio9E2Bnmd1Vs130_provenance; np:hasPublicationInfo dgn-np:NP335093.RA-FSlnw04nALJD_z_04HRQpf4jH3y6xGio9E2Bnmd1Vs130_publicationInfo; a np:Nanopublication . dgn-np:NP335093.RA-FSlnw04nALJD_z_04HRQpf4jH3y6xGio9E2Bnmd1Vs130_assertion a np:Assertion . dgn-np:NP335093.RA-FSlnw04nALJD_z_04HRQpf4jH3y6xGio9E2Bnmd1Vs130_provenance a np:Provenance . dgn-np:NP335093.RA-FSlnw04nALJD_z_04HRQpf4jH3y6xGio9E2Bnmd1Vs130_publicationInfo a np:PublicationInfo . } dgn-np:NP335093.RA-FSlnw04nALJD_z_04HRQpf4jH3y6xGio9E2Bnmd1Vs130_assertion { miriam-gene:4360 a ncit:C16612 . lld:C0007102 a ncit:C7057 . dgn-gda:DGN672f286dbad3d88884176ddbe73afd27 sio:SIO_000628 miriam-gene:4360, lld:C0007102; a sio:SIO_001121 . } dgn-np:NP335093.RA-FSlnw04nALJD_z_04HRQpf4jH3y6xGio9E2Bnmd1Vs130_provenance { dgn-np:NP335093.RA-FSlnw04nALJD_z_04HRQpf4jH3y6xGio9E2Bnmd1Vs130_assertion dcterms:description "[In this report, we show that such hybrid cell lines can also be a valuable tool in the study of the mutated MMR proteins, in particular the variants found in hereditary nonpolyposis colon cancer families that carry missense mutations and where it is unclear whether they predispose to colon 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:11691782; 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:NP335093.RA-FSlnw04nALJD_z_04HRQpf4jH3y6xGio9E2Bnmd1Vs130_publicationInfo { this: dcterms:created "2016-05-13T12:44:17+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }