Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_provenance.
- NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_assertion description "[De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_provenance.
- NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_assertion evidence source_evidence_literature NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_provenance.
- NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_assertion SIO_000772 26340335 NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_provenance.
- NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_assertion wasDerivedFrom befree-2016 NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_provenance.
- NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_assertion wasGeneratedBy ECO_0000203 NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293699.RAEJE1mfVKkAUWk1_5Zw4UH4TXoGwWBHwlCeCHG0DscKw130_provenance.