Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_provenance.
- NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_assertion description "[Split hand/split foot malformation (SHFM; ectrodactyly) is genetically heterogeneous, with mutations identified at five loci (SHFM1 at 7q21.3, SHFM2 at Xq26, SHFM3 at 10q24, SHFM4 at 3q27 and SHFM5 at 2q31).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_provenance.
- NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_assertion evidence source_evidence_literature NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_provenance.
- NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_assertion SIO_000772 15232212 NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_provenance.
- NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_assertion wasDerivedFrom befree-2016 NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_provenance.
- NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_assertion wasGeneratedBy ECO_0000203 NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_provenance.
- befree-2016 importedOn "2016-02-19" NP450639.RAbJAwxYgLtVN-2Py4CxUqrJx9hZfZscyL6bUW0_8lw_s130_provenance.