Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance.
- NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_assertion description "[Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance.
- NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_assertion evidence source_evidence_literature NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance.
- NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_assertion SIO_000772 15705923 NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance.
- NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_assertion wasDerivedFrom befree-20140225 NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance.
- NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_assertion wasGeneratedBy ECO_0000203 NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance.