Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_provenance.
- NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_assertion description "[The merosin (laminin alpha2 chain) deficient form (MDC1A), is characterized clinically by neonatal hypotonia, delayed motor milestones and associated contractures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_provenance.
- NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_assertion evidence source_evidence_literature NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_provenance.
- NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_assertion SIO_000772 16084089 NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_provenance.
- NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_assertion wasDerivedFrom befree-20140225 NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_provenance.
- NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_assertion wasGeneratedBy ECO_0000203 NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP565008.RAyUp9WRulCusnwf6SSj0LIvDviCxCZ_AhgWdU5uN8cHo130_provenance.