Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_provenance.
- NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_assertion description "[Molecular identification of hereditary persistence of fetal hemoglobin type 2 (HPFH type 2) in patients from Brazil.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_provenance.
- NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_assertion evidence source_evidence_literature NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_provenance.
- NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_assertion SIO_000772 7536477 NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_provenance.
- NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_assertion wasDerivedFrom befree-20150227 NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_provenance.
- NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_assertion wasGeneratedBy ECO_0000203 NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP786595.RAj5dwUmJJMAIntPo_N69mTlok69FbhY15aOvQWFFoQRM130_provenance.