Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_provenance.
- NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_assertion description "[A novel mutation in MIP associated with congenital nuclear cataract in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_provenance.
- NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_assertion evidence source_evidence_literature NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_provenance.
- NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_assertion SIO_000772 21245956 NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_provenance.
- NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_assertion wasDerivedFrom befree-20140225 NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_provenance.
- NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_assertion wasGeneratedBy ECO_0000203 NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP773897.RAkPIxNpq9Q5Zf2BBqL5Pic197CJ3t2WULbo2l7PAs0Hw130_provenance.