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- source_evidence_literature type ECO_0000212 NP541549.RAsn4Ux-PY56SmgwVa4MS97I4oy0CrRoXxsmnUYD-cX_g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541549.RAsn4Ux-PY56SmgwVa4MS97I4oy0CrRoXxsmnUYD-cX_g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541549.RAsn4Ux-PY56SmgwVa4MS97I4oy0CrRoXxsmnUYD-cX_g130_provenance.
- NP541549.RAsn4Ux-PY56SmgwVa4MS97I4oy0CrRoXxsmnUYD-cX_g130_assertion description "[By using multiple polymerase reaction (mPCR) and haploid analysis of 11 short tandem repeats (STRs) in dystrophin gene locus to identify female carriers in deletional DMD/BMD (Duchenne/Becker Muscular Dystrophy) families, valuable information can be gathered for prenatal diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541549.RAsn4Ux-PY56SmgwVa4MS97I4oy0CrRoXxsmnUYD-cX_g130_provenance.
- NP541549.RAsn4Ux-PY56SmgwVa4MS97I4oy0CrRoXxsmnUYD-cX_g130_assertion evidence source_evidence_literature NP541549.RAsn4Ux-PY56SmgwVa4MS97I4oy0CrRoXxsmnUYD-cX_g130_provenance.
- NP541549.RAsn4Ux-PY56SmgwVa4MS97I4oy0CrRoXxsmnUYD-cX_g130_assertion SIO_000772 16553208 NP541549.RAsn4Ux-PY56SmgwVa4MS97I4oy0CrRoXxsmnUYD-cX_g130_provenance.
- NP541549.RAsn4Ux-PY56SmgwVa4MS97I4oy0CrRoXxsmnUYD-cX_g130_assertion wasDerivedFrom befree-2016 NP541549.RAsn4Ux-PY56SmgwVa4MS97I4oy0CrRoXxsmnUYD-cX_g130_provenance.
- NP541549.RAsn4Ux-PY56SmgwVa4MS97I4oy0CrRoXxsmnUYD-cX_g130_assertion wasGeneratedBy ECO_0000203 NP541549.RAsn4Ux-PY56SmgwVa4MS97I4oy0CrRoXxsmnUYD-cX_g130_provenance.
- befree-2016 importedOn "2016-02-19" NP541549.RAsn4Ux-PY56SmgwVa4MS97I4oy0CrRoXxsmnUYD-cX_g130_provenance.