Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_provenance.
- NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_assertion description "[Different loci have been Identified for ectrodactyly (SHFM1 at 7q21.3q22.1, SHFM2 at Xq26, SHFM3 at 10q24q25, SHFM4 at 3q27), and two genes are known (DSS1 for SHFM1, p63 for SHFM4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_provenance.
- NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_assertion evidence source_evidence_literature NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_provenance.
- NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_assertion SIO_000772 12416640 NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_provenance.
- NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_assertion wasDerivedFrom befree-20150227 NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_provenance.
- NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_assertion wasGeneratedBy ECO_0000203 NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP767923.RAPnCL0P1w_M4XuGOZKKhqBB5D_XfcSuev6s0LLMaUoCw130_provenance.