Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_provenance.
- NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_assertion description "[In addition, they not only indicate that LMNA and TTN mutational status may be useful in this family for risk stratification in individuals at risk for DCM but also suggest titin as a modifier for DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_provenance.
- NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_assertion evidence source_evidence_literature NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_provenance.
- NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_assertion SIO_000772 23463027 NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_provenance.
- NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_assertion wasDerivedFrom befree-2016 NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_provenance.
- NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_assertion wasGeneratedBy ECO_0000203 NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1058050.RAomo-ctZl4mNYrcgqpA_PY42GLYt77mUXcH4sDSccfBs130_provenance.