Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_provenance.
- NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_assertion description "[Genetic heterogeneity of the PPR is obvious because the PPR also can be evoked in a number of autosomal recessive diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_provenance.
- NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_assertion evidence source_evidence_literature NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_provenance.
- NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_assertion SIO_000772 14706040 NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_provenance.
- NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_assertion wasDerivedFrom befree-20140225 NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_provenance.
- NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_assertion wasGeneratedBy ECO_0000203 NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_provenance.
- befree-20140225 importedOn "2014-02-25" NP154904.RAqBFlAItk80r88Iz9s4GROQgx3Ic5mdgHMHgo55Dhlys130_provenance.