Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP300414.RA4SLgos3empWIA4-g5oEFXgPZEYxRIeN7h7jeSTbSLac130_provenance.