Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_provenance.
- NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_assertion description "[Mutational spectrum in the PEX7 gene and functional analysis of mutant alleles in 78 patients with rhizomelic chondrodysplasia punctata type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_provenance.
- NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_assertion evidence source_evidence_literature NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_provenance.
- NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_assertion SIO_000772 11781871 NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_provenance.
- NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_assertion wasDerivedFrom befree-20150227 NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_provenance.
- NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_assertion wasGeneratedBy ECO_0000203 NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP616322.RAV7WUxP73euS9HipSRI0_Q--FmwJ4bMkDU-3CMHp1_aw130_provenance.