Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_provenance.
- NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_assertion description "[In the last year or so, mutations were discovered in differentiation specific keratins K6a and K16 causing pachyonychia congenita type 1 and K17 mutations occur in pachyonychia congenita type 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_provenance.
- NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_assertion evidence source_evidence_literature NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_provenance.
- NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_assertion SIO_000772 9028791 NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_provenance.
- NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_assertion wasDerivedFrom befree-20140225 NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_provenance.
- NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_assertion wasGeneratedBy ECO_0000203 NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP848022.RAO_pEXueezFxRwbaxKieqdgsKbVwB6krh94g_qfVxwHM130_provenance.