Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_provenance.
- NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_assertion description "[HMSN type II (HMSN II) or CMT2, the axonal form of CMT, is genetically heterogeneous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_provenance.
- NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_assertion evidence source_evidence_literature NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_provenance.
- NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_assertion SIO_000772 9595994 NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_provenance.
- NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_assertion wasDerivedFrom befree-20140225 NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_provenance.
- NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_assertion wasGeneratedBy ECO_0000203 NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP889987.RAlOU_ahbpdjAr6HZxN45H2YYluMUZ7Pv0Zf4Tn0wiOy4130_provenance.