Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_provenance.
- NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_assertion description "[Having explained the digital findings and macrocephaly, the skeletal changes were thought to fit best congenital spondyloepiphyseal dysplasia (SEDC MIM #183900), a type II collagen disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_provenance.
- NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_assertion evidence source_evidence_literature NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_provenance.
- NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_assertion SIO_000772 10678662 NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_provenance.
- NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_assertion wasDerivedFrom befree-20140225 NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_provenance.
- NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_assertion wasGeneratedBy ECO_0000203 NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP588828.RAYtq6PG8vpW5PthHDOPGbBun3ILlpVnBd5xDLTAyWFr4130_provenance.