Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.
- NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_assertion wasGeneratedBy ECO_0000203 NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.
- NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_assertion wasDerivedFrom befree-20140225 NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.
- NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_assertion SIO_000772 15776429 NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.
- NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_assertion evidence source_evidence_literature NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.
- NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_assertion description "[Recently, SIMPLE/LITAF was shown to be responsible for an autosomal dominant demyelinating form of CMT linked to 16p (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.