Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_provenance.
- NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_assertion description "[These results allow further delineation of the spectrum of malformations ascribed to SMADIP1 haploinsufficiency, which includes frequent features such as hypospadias and agenesis of the corpus callosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_provenance.
- NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_assertion evidence source_evidence_literature NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_provenance.
- NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_assertion SIO_000772 11595972 NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_provenance.
- NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_assertion wasDerivedFrom befree-2016 NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_provenance.
- NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_assertion wasGeneratedBy ECO_0000203 NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_provenance.
- befree-2016 importedOn "2016-02-19" NP332857.RAllDwhTbUv1aHLiCm5vo-TLcasvTAqi4LXlk-KGY8B-k130_provenance.