Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance.
- NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_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." NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance.
- NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_assertion evidence source_evidence_literature NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance.
- NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_assertion SIO_000772 15705923 NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance.
- NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_assertion wasDerivedFrom befree-20150227 NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance.
- NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_assertion wasGeneratedBy ECO_0000203 NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance.