Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_assertion> ?p ?o ?g. }
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- NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_assertion type Assertion NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_head.
- NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_assertion wasGeneratedBy ECO_0000203 NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_provenance.
- NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_assertion wasDerivedFrom befree-20140225 NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_provenance.
- NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_assertion SIO_000772 23428682 NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_provenance.
- NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_assertion evidence source_evidence_literature NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_provenance.
- NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_assertion description "[A patient with a mutation that led to a partially functional protein had a less severe growth phenotype and no deafness, similarly to two siblings with a heterozygous IGF1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_provenance.