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- source_evidence_literature type ECO_0000212 NP775305.RA33oZmYajPcaWw1CGH88kFEsen44UAc98Or_2MmoAZfE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775305.RA33oZmYajPcaWw1CGH88kFEsen44UAc98Or_2MmoAZfE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775305.RA33oZmYajPcaWw1CGH88kFEsen44UAc98Or_2MmoAZfE130_provenance.
- NP775305.RA33oZmYajPcaWw1CGH88kFEsen44UAc98Or_2MmoAZfE130_assertion description "[Here we report the experience of our group in the counselling and molecular prenatal diagnosis of three inherited neuromuscular diseases, i.e., Duchenne/Becker muscular dystrophy (DMD/BMD), myotonic dystrophy type 1 (DM1), spinal muscular atrophy (SMA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775305.RA33oZmYajPcaWw1CGH88kFEsen44UAc98Or_2MmoAZfE130_provenance.
- NP775305.RA33oZmYajPcaWw1CGH88kFEsen44UAc98Or_2MmoAZfE130_assertion evidence source_evidence_literature NP775305.RA33oZmYajPcaWw1CGH88kFEsen44UAc98Or_2MmoAZfE130_provenance.
- NP775305.RA33oZmYajPcaWw1CGH88kFEsen44UAc98Or_2MmoAZfE130_assertion SIO_000772 23729582 NP775305.RA33oZmYajPcaWw1CGH88kFEsen44UAc98Or_2MmoAZfE130_provenance.
- NP775305.RA33oZmYajPcaWw1CGH88kFEsen44UAc98Or_2MmoAZfE130_assertion wasDerivedFrom befree-20150227 NP775305.RA33oZmYajPcaWw1CGH88kFEsen44UAc98Or_2MmoAZfE130_provenance.
- NP775305.RA33oZmYajPcaWw1CGH88kFEsen44UAc98Or_2MmoAZfE130_assertion wasGeneratedBy ECO_0000203 NP775305.RA33oZmYajPcaWw1CGH88kFEsen44UAc98Or_2MmoAZfE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP775305.RA33oZmYajPcaWw1CGH88kFEsen44UAc98Or_2MmoAZfE130_provenance.