Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_provenance.
- NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_assertion description "[The syndrome of IAHSP is genetically heterogeneous, and no clinical sign can help to distinguish patients with and without Alsin mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_provenance.
- NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_assertion evidence source_evidence_literature NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_provenance.
- NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_assertion SIO_000772 12601111 NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_provenance.
- NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_assertion wasDerivedFrom befree-2016 NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_provenance.
- NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_assertion wasGeneratedBy ECO_0000203 NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_provenance.
- befree-2016 importedOn "2016-02-19" NP384698.RAzEPgEzuyuW2HbsCuIy7TCZgA9EDYXd_sVPPvsoslMZ8130_provenance.