Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP741669.RABTe7HZhXL6OmHnjrGzKLgDZ8GnwDmbaSFc47cZwbpns130_assertion> ?p ?o ?g. }
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- NP741669.RABTe7HZhXL6OmHnjrGzKLgDZ8GnwDmbaSFc47cZwbpns130_assertion type Assertion NP741669.RABTe7HZhXL6OmHnjrGzKLgDZ8GnwDmbaSFc47cZwbpns130_head.
- NP741669.RABTe7HZhXL6OmHnjrGzKLgDZ8GnwDmbaSFc47cZwbpns130_assertion wasGeneratedBy ECO_0000203 NP741669.RABTe7HZhXL6OmHnjrGzKLgDZ8GnwDmbaSFc47cZwbpns130_provenance.
- NP741669.RABTe7HZhXL6OmHnjrGzKLgDZ8GnwDmbaSFc47cZwbpns130_assertion wasDerivedFrom befree-20140225 NP741669.RABTe7HZhXL6OmHnjrGzKLgDZ8GnwDmbaSFc47cZwbpns130_provenance.
- NP741669.RABTe7HZhXL6OmHnjrGzKLgDZ8GnwDmbaSFc47cZwbpns130_assertion SIO_000772 23957197 NP741669.RABTe7HZhXL6OmHnjrGzKLgDZ8GnwDmbaSFc47cZwbpns130_provenance.
- NP741669.RABTe7HZhXL6OmHnjrGzKLgDZ8GnwDmbaSFc47cZwbpns130_assertion evidence source_evidence_literature NP741669.RABTe7HZhXL6OmHnjrGzKLgDZ8GnwDmbaSFc47cZwbpns130_provenance.
- NP741669.RABTe7HZhXL6OmHnjrGzKLgDZ8GnwDmbaSFc47cZwbpns130_assertion description "[Human insulin like growth factor (IGF) I deficiency is a rare disease associated with hearing loss, poor growth rates and mental retardation (ORPHA73272, OMIM608747).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP741669.RABTe7HZhXL6OmHnjrGzKLgDZ8GnwDmbaSFc47cZwbpns130_provenance.