Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_provenance.
- NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_assertion description "[Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_provenance.
- NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_assertion evidence source_evidence_literature NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_provenance.
- NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_assertion SIO_000772 20137778 NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_provenance.
- NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_assertion wasDerivedFrom befree-20150227 NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_provenance.
- NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_assertion wasGeneratedBy ECO_0000203 NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP990460.RAZiOvaVYebBWREfkXp9eMer8UTdTV_P7QUKCQ4Fjync8130_provenance.