Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_provenance.
- NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_assertion description "[While double knockout of Dlx5 and Dlx6 resulted in limb defects in mice, the majority of patients with SHFM1 had only heterozygous chromosomal abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_provenance.
- NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_assertion evidence source_evidence_literature NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_provenance.
- NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_assertion SIO_000772 25332435 NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_provenance.
- NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_assertion wasDerivedFrom befree-2016 NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_provenance.
- NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_assertion wasGeneratedBy ECO_0000203 NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1231036.RAOyWjD7Qp1NqEo3LhMugY0PfttRFhy7dkHtI55Trnhfo130_provenance.