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- source_evidence_literature type ECO_0000212 NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_provenance.
- NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_assertion description "[Merosin (laminin-2 and -4; alpha 2-beta 1/beta 2-gamma 1) is the predominant laminin variant in skeletal muscle basement membranes; genetic defects affecting its structure or expression are the causes of some types of congenital muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_provenance.
- NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_assertion evidence source_evidence_literature NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_provenance.
- NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_assertion SIO_000772 8830776 NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_provenance.
- NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_assertion wasDerivedFrom befree-2016 NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_provenance.
- NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_assertion wasGeneratedBy ECO_0000203 NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_provenance.
- befree-2016 importedOn "2016-02-19" NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_provenance.