Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_provenance.
- NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_assertion description "[The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disorder caused by mutations of a member of the GATA-binding family of transcription factors, GATA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_provenance.
- NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_assertion evidence source_evidence_literature NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_provenance.
- NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_assertion SIO_000772 15705923 NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_provenance.
- NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_assertion wasDerivedFrom befree-2016 NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_provenance.
- NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_assertion wasGeneratedBy ECO_0000203 NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_provenance.
- befree-2016 importedOn "2016-02-19" NP480538.RAE5np7Pshlota0vJnY0hFX1s7_XjVh7ZWvv-GU79s1AU130_provenance.