Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_provenance.
- NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_assertion description "[Based on these observations, an autosomal dominant form of ectrodactyly is assumed to reside in this region and the locus has been designated SHFD1 (split hand/split foot disorder).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_provenance.
- NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_assertion evidence source_evidence_literature NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_provenance.
- NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_assertion SIO_000772 7987314 NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_provenance.
- NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_assertion wasDerivedFrom befree-2016 NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_provenance.
- NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_assertion wasGeneratedBy ECO_0000203 NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1329167.RAK_SUhSTa4iWDBp6mHhQ4NpBbHFCL8Utq0Bqvb1SXFOE130_provenance.