Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_provenance.
- NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_assertion description "[Mutations in the heparan-sulfate proteoglycan glypican 6 (GPC6) impair endochondral ossification and cause recessive omodysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_provenance.
- NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_assertion evidence source_evidence_literature NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_provenance.
- NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_assertion SIO_000772 19481194 NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_provenance.
- NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_assertion wasDerivedFrom befree-2016 NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_provenance.
- NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_assertion wasGeneratedBy ECO_0000203 NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_provenance.
- befree-2016 importedOn "2016-02-19" NP741961.RAx-CWPQv63EpelW7rhaJZlIPQ5BEkPE6gUHJlrM3Z8hI130_provenance.