Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_provenance.
- NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_assertion description "[However, previous mutation analysis of the coding sequence of the HOX11L1 gene in patients affected with IND detected neither mutations nor other nucleotide variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_provenance.
- NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_assertion evidence source_evidence_literature NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_provenance.
- NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_assertion SIO_000772 12060859 NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_provenance.
- NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_assertion wasDerivedFrom befree-2016 NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_provenance.
- NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_assertion wasGeneratedBy ECO_0000203 NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_provenance.
- befree-2016 importedOn "2016-02-19" NP357617.RARJL-P0zpQmDtISIDLBPFAO2zpN5EF0oboRmw3CeDX-U130_provenance.