Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_provenance.
- NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_assertion description "[Interestingly the ALP gene occurs at 4q35 near the heterochromatic region mutated in facioscapulohumeral muscular dystrophy, indicating a possible role for ALP in this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_provenance.
- NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_assertion evidence source_evidence_literature NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_provenance.
- NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_assertion SIO_000772 11238905 NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_provenance.
- NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_assertion wasDerivedFrom befree-20140225 NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_provenance.
- NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_assertion wasGeneratedBy ECO_0000203 NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP637223.RAwRZLXz8IRpRYH5Xjmk7CVxBqkA5ktKY0QpdiVSIVjUo130_provenance.