Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_provenance.
- NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_assertion description "[Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_provenance.
- NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_assertion evidence source_evidence_literature NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_provenance.
- NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_assertion SIO_000772 17236138 NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_provenance.
- NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_assertion wasDerivedFrom befree-20140225 NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_provenance.
- NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_assertion wasGeneratedBy ECO_0000203 NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP734355.RAC2IiixzDjllIBqZroceiTdMF6s2gSfekyi1RoHTnGLs130_provenance.