Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.
- NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_assertion wasGeneratedBy ECO_0000203 NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.
- NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_assertion wasDerivedFrom befree-20150227 NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.
- NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_assertion SIO_000772 24405844 NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.
- NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_assertion evidence source_evidence_literature NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.
- NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_assertion description "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556873.RABwMltYbRRUirtqHz3mx4IRs4Mwvta4H5LVIWIf5Nv4g130_provenance.