Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_provenance.
- NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_assertion wasGeneratedBy ECO_0000203 NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_provenance.
- NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_assertion wasDerivedFrom befree-20140225 NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_provenance.
- NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_assertion SIO_000772 12383326 NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_provenance.
- NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_assertion evidence source_evidence_literature NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_provenance.
- NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_assertion description "[The principal features of CCA are a marfanoid habitus, multiple congenital contractures, camptodactyly, arachnodactyly, kyphoscoliosis, muscular hypoplasia, and external ear malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP516100.RAdyjK0aXvyqwIvbfEhq1Ftq3xLc3cgE7D9-MfLAhckIo130_provenance.