Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance.
- NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_assertion description "[A 263 Kb homozygous deletion of FMN1 was associated with oligosyndactyly, radioulnar synostosis, hearing loss and renal defects, features identical to ld mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance.
- NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_assertion evidence source_evidence_literature NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance.
- NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_assertion SIO_000772 20610440 NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance.
- NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_assertion wasDerivedFrom befree-20140225 NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance.
- NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_assertion wasGeneratedBy ECO_0000203 NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance.
- befree-20140225 importedOn "2014-02-25" NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance.